US6752947B1 - Method and apparatus for thermal bonding high elongation nonwoven fabric - Google Patents

Method and apparatus for thermal bonding high elongation nonwoven fabric Download PDF

Info

Publication number
US6752947B1
US6752947B1 US09/116,371 US11637198A US6752947B1 US 6752947 B1 US6752947 B1 US 6752947B1 US 11637198 A US11637198 A US 11637198A US 6752947 B1 US6752947 B1 US 6752947B1
Authority
US
United States
Prior art keywords
lands
machine direction
fibers
adjacent rows
fiber
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Expired - Lifetime, expires
Application number
US09/116,371
Inventor
William Robert Lanigan
Richard J. Legare
Shiv Sibal
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Fibervisions Lp
Hercules LLC
Original Assignee
Hercules LLC
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Hercules LLC filed Critical Hercules LLC
Priority to US09/116,371 priority Critical patent/US6752947B1/en
Assigned to FIBERVISIONS INCORPORATED reassignment FIBERVISIONS INCORPORATED ASSIGNMENT OF ASSIGNORS INTEREST (SEE DOCUMENT FOR DETAILS). Assignors: LEGARE, RICHARD J., SIBAL, SHIV, LANIGAN, WILLIAM ROBERT
Priority to CN99810479A priority patent/CN1321119A/en
Priority to CA002336834A priority patent/CA2336834A1/en
Priority to AU49533/99A priority patent/AU4953399A/en
Priority to EP99933486A priority patent/EP1144741A3/en
Priority to JP2000560304A priority patent/JP2002522648A/en
Priority to PCT/US1999/012370 priority patent/WO2000004215A2/en
Assigned to BANK OF AMERICA, N.A., AS COLLATERAL AGENT reassignment BANK OF AMERICA, N.A., AS COLLATERAL AGENT NOTICE OF GRANT OF SECURITY INTEREST Assignors: AQUALON COMPANY, ATHENS HOLDINGS, INC., BETZDEARBORN CHINA, LTD., BETZDEARBORN EUROPE, INC., BETZDEARBORN INC., BETZDEARBORN INTERNATIONAL, INC., BL CHEMICALS INC., BL TECHNOLOGIES, INC., BLI HOLDINGS CORP., CHEMICAL TECHNOLOGIES INDIA, LTD., COVINGTON HOLDINGS, INC., D R C LTD., EAST BAY REALTY SERVICES, INC., FIBERVISIONS INCORPORATED, FIBERVISIONS PRODUCTS, INC., FIBERVISIONS, L.L.C., FIBERVISIONS, L.P., HERCULES CHEMICAL CORPORATION, HERCULES COUNTRY CLUB, INC., HERCULES CREDIT, INC., HERCULES EURO HOLDINGS, LLC, HERCULES FINANCE COMPANY, HERCULES FLAVOR, INC., HERCULES INCORPORATED, HERCULES INTERNATIONAL LIMITED, HERCULES INTERNATIONAL LIMITED, L.L.C., HERCULES INVESTMENTS, LLC, HERCULES SHARED SERVICES CORPORATION, HISPAN CORPORATION, WSP, INC.
Assigned to CREDIT SUISSE FIRST BOSTON, AS COLLATERAL AGENT reassignment CREDIT SUISSE FIRST BOSTON, AS COLLATERAL AGENT SECURITY INTEREST (SEE DOCUMENT FOR DETAILS). Assignors: HERCULES INCORPORATED
Assigned to BLI HOLDING CORPORATION, HERCULES COUNTRY CLUB, INC., EAST BAY REALTY SERVICES, INC., BL CHEMICALS INC., BETZDEARBORN CHINA, LTD., WSP, INC., FIBERVISIONS, L.P., HERCULES CREDIT, INC., HERCULES EURO HOLDINGS, LLC, BETZDEARBORN, INC., D R C LTD., HERCULES SHARED SERVICES CORPORATION, FIBERVISIONS PRODUCTS, INC., BETZDEARBORN EUROPE, INC., COVINGTON HOLDINGS, INC., FIBERVISIONS, L.L.C., HERCULES CHEMICAL CORPORATION, CHEMICAL TECHNOLOGIES INDIA, LTD., HERCULES INTERNATIONAL LIMITED, ATHENS HOLDINGS, INC., HERCULES INCORPORATED, BL TECHNOLOGIES, INC., HERCULES FLAVOR, INC., HERCULES FINANCE COMPANY, AQUALON COMPANY, BETZDEARBORN INTERNATIONAL, INC., HERCULES INVESTMENTS, LLC, FIBERVISIONS INCORPORATED, HERCULES INTERNATIONAL LIMITED, L.L.C., HISPAN CORPORATION reassignment BLI HOLDING CORPORATION RELEASE OF SECURITY INTEREST Assignors: BANK OF AMERICA, N.A., AS COLLATERAL AGENT
Publication of US6752947B1 publication Critical patent/US6752947B1/en
Application granted granted Critical
Assigned to CREDIT SUISSE reassignment CREDIT SUISSE SECOND LIEN SECURITY AGREEMENT Assignors: FIBERVISIONS, L.P.
Assigned to CREDIT SUISSE reassignment CREDIT SUISSE FIRST LIEN SECURITY AGREEMENT Assignors: FIBERVISIONS, L.P.
Assigned to HERCULES INCORPORATED reassignment HERCULES INCORPORATED RELEASE BY SECURED PARTY (SEE DOCUMENT FOR DETAILS). Assignors: CREDIT SUISSE
Assigned to HERCULES INCORPORATED reassignment HERCULES INCORPORATED PATENT TERMINATION CS-013625-0233 Assignors: CREDIT SUISSE, CAYMAN ISLANDS BRANCH
Assigned to BANK OF AMERICA, N.A., AS ADMINISTRATIVE AGENT reassignment BANK OF AMERICA, N.A., AS ADMINISTRATIVE AGENT NOTICE OF GRANT OF SECURITY INTEREST IN PATENTS Assignors: FIBERVISIONS L.P.
Assigned to FIBERVISIONS, L.P. reassignment FIBERVISIONS, L.P. RELEASE OF FIRST LIEN SECURITY INTEREST IN INTELLECTUAL PROPERTY COLLATERAL AT REEL/FRAME NO. 17537/0201 Assignors: CREDIT SUISSE AG, CAYMAN ISLANDS BRANCH (F/K/A CREDIT SUISSE, CAYMAN ISLANDS BRANCH)
Assigned to FIBERVISIONS, L.P. reassignment FIBERVISIONS, L.P. RELEASE OF SECOND LIEN SECURITY INTEREST IN INTELLECTUAL PROPERTY COLLATERAL AT REEL/FRAME NO. 17537/0220 Assignors: CREDIT SUISSE AG, CAYMAN ISLANDS BRANCH (F/K/A CREDIT SUISSE, CAYMAN ISLANDS BRANCH)
Assigned to FIBERVISIONS MANUFACTURING COMPANY reassignment FIBERVISIONS MANUFACTURING COMPANY CHANGE OF NAME (SEE DOCUMENT FOR DETAILS). Assignors: FIBERVISIONS INCORPORATED
Assigned to FIBERVISIONS, L.P. reassignment FIBERVISIONS, L.P. ASSIGNMENT OF ASSIGNORS INTEREST (SEE DOCUMENT FOR DETAILS). Assignors: FIBERVISIONS MANUFACTURING COMPANY
Assigned to FIBERVISIONS, L.P. reassignment FIBERVISIONS, L.P. TERMINATION AND RELEASE OF SECURITY INTEREST IN PATENTS Assignors: BANK OF AMERICA, N.A., AS ADMINISTRATIVE AGENT
Adjusted expiration legal-status Critical
Expired - Lifetime legal-status Critical Current

Links

Images

Classifications

    • DTEXTILES; PAPER
    • D04BRAIDING; LACE-MAKING; KNITTING; TRIMMINGS; NON-WOVEN FABRICS
    • D04HMAKING TEXTILE FABRICS, e.g. FROM FIBRES OR FILAMENTARY MATERIAL; FABRICS MADE BY SUCH PROCESSES OR APPARATUS, e.g. FELTS, NON-WOVEN FABRICS; COTTON-WOOL; WADDING ; NON-WOVEN FABRICS FROM STAPLE FIBRES, FILAMENTS OR YARNS, BONDED WITH AT LEAST ONE WEB-LIKE MATERIAL DURING THEIR CONSOLIDATION
    • D04H3/00Non-woven fabrics formed wholly or mainly of yarns or like filamentary material of substantial length
    • D04H3/08Non-woven fabrics formed wholly or mainly of yarns or like filamentary material of substantial length characterised by the method of strengthening or consolidating
    • D04H3/14Non-woven fabrics formed wholly or mainly of yarns or like filamentary material of substantial length characterised by the method of strengthening or consolidating with bonds between thermoplastic yarns or filaments produced by welding
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61FFILTERS IMPLANTABLE INTO BLOOD VESSELS; PROSTHESES; DEVICES PROVIDING PATENCY TO, OR PREVENTING COLLAPSING OF, TUBULAR STRUCTURES OF THE BODY, e.g. STENTS; ORTHOPAEDIC, NURSING OR CONTRACEPTIVE DEVICES; FOMENTATION; TREATMENT OR PROTECTION OF EYES OR EARS; BANDAGES, DRESSINGS OR ABSORBENT PADS; FIRST-AID KITS
    • A61F13/00Bandages or dressings; Absorbent pads
    • A61F13/15Absorbent pads, e.g. sanitary towels, swabs or tampons for external or internal application to the body; Supporting or fastening means therefor; Tampon applicators
    • A61F13/15577Apparatus or processes for manufacturing
    • A61F13/15707Mechanical treatment, e.g. notching, twisting, compressing, shaping
    • A61F13/15731Treating webs, e.g. for giving them a fibrelike appearance, e.g. by embossing
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B29WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
    • B29CSHAPING OR JOINING OF PLASTICS; SHAPING OF MATERIAL IN A PLASTIC STATE, NOT OTHERWISE PROVIDED FOR; AFTER-TREATMENT OF THE SHAPED PRODUCTS, e.g. REPAIRING
    • B29C59/00Surface shaping of articles, e.g. embossing; Apparatus therefor
    • B29C59/02Surface shaping of articles, e.g. embossing; Apparatus therefor by mechanical means, e.g. pressing
    • B29C59/022Surface shaping of articles, e.g. embossing; Apparatus therefor by mechanical means, e.g. pressing characterised by the disposition or the configuration, e.g. dimensions, of the embossments or the shaping tools therefor
    • DTEXTILES; PAPER
    • D04BRAIDING; LACE-MAKING; KNITTING; TRIMMINGS; NON-WOVEN FABRICS
    • D04HMAKING TEXTILE FABRICS, e.g. FROM FIBRES OR FILAMENTARY MATERIAL; FABRICS MADE BY SUCH PROCESSES OR APPARATUS, e.g. FELTS, NON-WOVEN FABRICS; COTTON-WOOL; WADDING ; NON-WOVEN FABRICS FROM STAPLE FIBRES, FILAMENTS OR YARNS, BONDED WITH AT LEAST ONE WEB-LIKE MATERIAL DURING THEIR CONSOLIDATION
    • D04H1/00Non-woven fabrics formed wholly or mainly of staple fibres or like relatively short fibres
    • D04H1/40Non-woven fabrics formed wholly or mainly of staple fibres or like relatively short fibres from fleeces or layers composed of fibres without existing or potential cohesive properties
    • D04H1/42Non-woven fabrics formed wholly or mainly of staple fibres or like relatively short fibres from fleeces or layers composed of fibres without existing or potential cohesive properties characterised by the use of certain kinds of fibres insofar as this use has no preponderant influence on the consolidation of the fleece
    • D04H1/4282Addition polymers
    • D04H1/4291Olefin series
    • DTEXTILES; PAPER
    • D04BRAIDING; LACE-MAKING; KNITTING; TRIMMINGS; NON-WOVEN FABRICS
    • D04HMAKING TEXTILE FABRICS, e.g. FROM FIBRES OR FILAMENTARY MATERIAL; FABRICS MADE BY SUCH PROCESSES OR APPARATUS, e.g. FELTS, NON-WOVEN FABRICS; COTTON-WOOL; WADDING ; NON-WOVEN FABRICS FROM STAPLE FIBRES, FILAMENTS OR YARNS, BONDED WITH AT LEAST ONE WEB-LIKE MATERIAL DURING THEIR CONSOLIDATION
    • D04H1/00Non-woven fabrics formed wholly or mainly of staple fibres or like relatively short fibres
    • D04H1/40Non-woven fabrics formed wholly or mainly of staple fibres or like relatively short fibres from fleeces or layers composed of fibres without existing or potential cohesive properties
    • D04H1/54Non-woven fabrics formed wholly or mainly of staple fibres or like relatively short fibres from fleeces or layers composed of fibres without existing or potential cohesive properties by welding together the fibres, e.g. by partially melting or dissolving
    • D04H1/542Adhesive fibres
    • D04H1/544Olefin series
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B29WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
    • B29KINDEXING SCHEME ASSOCIATED WITH SUBCLASSES B29B, B29C OR B29D, RELATING TO MOULDING MATERIALS OR TO MATERIALS FOR MOULDS, REINFORCEMENTS, FILLERS OR PREFORMED PARTS, e.g. INSERTS
    • B29K2105/00Condition, form or state of moulded material or of the material to be shaped
    • B29K2105/06Condition, form or state of moulded material or of the material to be shaped containing reinforcements, fillers or inserts
    • B29K2105/08Condition, form or state of moulded material or of the material to be shaped containing reinforcements, fillers or inserts of continuous length, e.g. cords, rovings, mats, fabrics, strands or yarns
    • B29K2105/0854Condition, form or state of moulded material or of the material to be shaped containing reinforcements, fillers or inserts of continuous length, e.g. cords, rovings, mats, fabrics, strands or yarns in the form of a non-woven mat
    • DTEXTILES; PAPER
    • D04BRAIDING; LACE-MAKING; KNITTING; TRIMMINGS; NON-WOVEN FABRICS
    • D04HMAKING TEXTILE FABRICS, e.g. FROM FIBRES OR FILAMENTARY MATERIAL; FABRICS MADE BY SUCH PROCESSES OR APPARATUS, e.g. FELTS, NON-WOVEN FABRICS; COTTON-WOOL; WADDING ; NON-WOVEN FABRICS FROM STAPLE FIBRES, FILAMENTS OR YARNS, BONDED WITH AT LEAST ONE WEB-LIKE MATERIAL DURING THEIR CONSOLIDATION
    • D04H1/00Non-woven fabrics formed wholly or mainly of staple fibres or like relatively short fibres
    • D04H1/40Non-woven fabrics formed wholly or mainly of staple fibres or like relatively short fibres from fleeces or layers composed of fibres without existing or potential cohesive properties
    • D04H1/42Non-woven fabrics formed wholly or mainly of staple fibres or like relatively short fibres from fleeces or layers composed of fibres without existing or potential cohesive properties characterised by the use of certain kinds of fibres insofar as this use has no preponderant influence on the consolidation of the fleece
    • D04H1/4382Stretched reticular film fibres; Composite fibres; Mixed fibres; Ultrafine fibres; Fibres for artificial leather
    • D04H1/43825Composite fibres
    • D04H1/43828Composite fibres sheath-core
    • DTEXTILES; PAPER
    • D04BRAIDING; LACE-MAKING; KNITTING; TRIMMINGS; NON-WOVEN FABRICS
    • D04HMAKING TEXTILE FABRICS, e.g. FROM FIBRES OR FILAMENTARY MATERIAL; FABRICS MADE BY SUCH PROCESSES OR APPARATUS, e.g. FELTS, NON-WOVEN FABRICS; COTTON-WOOL; WADDING ; NON-WOVEN FABRICS FROM STAPLE FIBRES, FILAMENTS OR YARNS, BONDED WITH AT LEAST ONE WEB-LIKE MATERIAL DURING THEIR CONSOLIDATION
    • D04H1/00Non-woven fabrics formed wholly or mainly of staple fibres or like relatively short fibres
    • D04H1/40Non-woven fabrics formed wholly or mainly of staple fibres or like relatively short fibres from fleeces or layers composed of fibres without existing or potential cohesive properties
    • D04H1/42Non-woven fabrics formed wholly or mainly of staple fibres or like relatively short fibres from fleeces or layers composed of fibres without existing or potential cohesive properties characterised by the use of certain kinds of fibres insofar as this use has no preponderant influence on the consolidation of the fleece
    • D04H1/4382Stretched reticular film fibres; Composite fibres; Mixed fibres; Ultrafine fibres; Fibres for artificial leather
    • D04H1/43838Ultrafine fibres, e.g. microfibres
    • YGENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10TECHNICAL SUBJECTS COVERED BY FORMER USPC
    • Y10TTECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
    • Y10T156/00Adhesive bonding and miscellaneous chemical manufacture
    • Y10T156/10Methods of surface bonding and/or assembly therefor
    • Y10T156/1002Methods of surface bonding and/or assembly therefor with permanent bending or reshaping or surface deformation of self sustaining lamina
    • Y10T156/1007Running or continuous length work
    • Y10T156/1023Surface deformation only [e.g., embossing]
    • YGENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10TECHNICAL SUBJECTS COVERED BY FORMER USPC
    • Y10TTECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
    • Y10T156/00Adhesive bonding and miscellaneous chemical manufacture
    • Y10T156/17Surface bonding means and/or assemblymeans with work feeding or handling means
    • Y10T156/1702For plural parts or plural areas of single part
    • Y10T156/1712Indefinite or running length work
    • Y10T156/1737Discontinuous, spaced area, and/or patterned pressing

Definitions

  • the present invention relates to thermal bonding of nonwoven fabric, especially high elongation nonwoven fabric, and to calender rolls for producing such nonwoven fabric as well as to nonwoven fabrics and articles including nonwoven fabrics.
  • Nonwoven fabrics are typically made by making a web, and then thermally bonding the fibers together.
  • staple fibers can be converted into nonwoven fabrics using, for example, a carding machine, and the carded fabric can be thermally bonded.
  • the thermal bonding can be achieved using various heating techniques, including heating with heated rollers, hot air and heating through the use of ultrasonic welding.
  • heated rollers When heated rollers are utilized to bond the carded fabric, typically there is utilized one roll that is smooth and a calender roll that includes bonding spots thereon.
  • the material to be thermally bonded is fed through a nip between the smooth roll and the calendar roll, with sufficient heat being applied to obtain thermal bonding of the material.
  • thermal bonding calender rolls such as embossed calender rolls, are configured with a plurality of lands to provide bonding spots to provide maximum machine direction strength and cross direction strength, while preferably providing a soft feel or touch to the material, especially when forming the thermal bonded material or fabric from synthetic materials.
  • thermal bonded fabric is often used to form nonwoven cover stock, which is typically used for hygiene products, such as a top sheet of a diaper.
  • cover stock material is placed in contact with a human body, for example, placed on the skin of a baby. Therefore, it is desirable that the face in contact with the human body exhibit softness.
  • the conventional processes utilize embossed thermal bonding calender rolls designed with a plurality of spaced lands that form bonding spots to provide a soft touch, as well as maximum machine direction and cross-direction strength.
  • embossed thermal bonding calender rolls designed with a plurality of spaced lands that form bonding spots to provide a soft touch, as well as maximum machine direction and cross-direction strength.
  • most of the prior art card-produced nonwoven fabrics do not have acceptable stretch characteristics.
  • the present invention provides a method of manufacturing thermally bonded fabric having high elongation, comprising forming a web of thermally bondable polypropylene fibers; passing the web over a heated calender roll having a patterned surface including a plurality of rows of lands, with each of the lands having an upper surface, with upper surfaces of lands in adjacent rows being staggered such that they do not overlap one another in a machine direction; and thermally bonding the fibers at bond points located about the upper surfaces of the lands such that fibers extending substantially in the machine direction will only have one bond point for adjacent rows.
  • the polypropylene fibers are preferably skin core polypropylene fibers.
  • the web can be provided as a carded fibrous web, or as a plurality of continuous filaments.
  • the elongation of the nonwoven fabric is at least about 120%, preferably greater than about 140%, more preferably greater than about 160%, even more preferably greater than about 180%, even more preferably greater than about 200%, even more preferably greater than about 250%, and most preferably greater than 300%.
  • the passing of the web over a heated calender roll can comprise passing the fibrous web between a pair of cooperating rolls in a calender nip, at least one of the pair of rolls having the patterned surface and comprising a cylindrical roll having an outer cylindrical surface including a plurality of lands; the lands being arranged on the outer cylindrical surface in a plurality of spaced apart rows; each of the lands comprising a tapered shape including a base, preferably substantially rectangular, tapering to an upper surface, which is preferably substantially rectangular; the upper surface including short sides oriented in the machine direction of about 0.036 cm to 0.066 cm in length, preferably about 0.043 cm to 0.059 cm, with a preferred value being about 0.051 cm, and long sides of about 0.071 cm to 0.133 cm in length oriented in a cross direction, preferably about 0.087 cm to 0.117 cm, with a preferred value being about 0.102 cm; adjacent rows of the lands being spaced apart a distance, with respect to the centers of the lands, of about
  • the upper surfaces of the lands can be substantially rectangular. Moreover, the bases can overlap in the machine direction in adjacent rows.
  • Centers of the lands in each row are spaced apart by a distance of about 0.142 cm to 0.264 cm, preferably about 0.173 cm to 0.233 cm, with a preferred value being about 0.203 cm, and centers of the lands in adjacent rows are spaced apart by a distance of about 0.071 cm to 0.133 cm, preferably about 0.087 cm to 0.117 cm, with a preferred value being about 0.102 cm.
  • the lands are constructed and arranged such that a straight fiber lying at an angle of greater than 15% with respect to the machine direction, more preferably about 35° to 55°, and even more preferably 45°, is positioned in a space between the lands, whereby the fiber is not be bonded.
  • the lands are preferably of a truncated pyramidal shape, preferably having substantially rectangular bases with short sides about 0.075 cm to 0.139 cm in length oriented in the machine direction, preferably 0.091 cm to 0.123 cm, with a preferred value being about 0.107 cm, and long sides about 0.111 cm to 0.205 cm in length oriented in the cross direction, preferably about 0.134 cm to 0.182 cm, with a preferred value being about 0.158 cm, and tapered side walls extending between the base and the upper surface at an angle a of about 14° to 35°, preferably about 17° to 26°, more preferably about 17° to 23°, with a preferred value being about 20°.
  • the lands can have a height of about 0.053 cm to 0.099 cm, preferably about 0.065 cm to 0.087 cm, with a preferred value being about 0.076 cm.
  • thermally bonded fabric having high elongation comprising forming a web comprising thermally bondable skin-core polypropylene fibers; passing the web over a calender roll having a patterned surface including a plurality of rows of lands, with each of the lands having an upper surface, with upper surfaces of lands in adjacent rows being staggered such that they do not overlap one another in a machine direction; applying heat and pressure to the fibrous web at a location of the calender roll to thermally bond the fibers at bond points located about the upper surfaces of the lands such that fibers extending substantially in the machine direction will only have one bond point for adjacent rows.
  • the present invention is also directed to the calender roll and to polypropylene fabrics formed by the methods.
  • FIG. 1 depicts a portion of the patterned calender roll according to the present invention, with the pattern broken away at the central portion;
  • FIG. 2 depicts the relative spacing of the lands forming the bond spots according to the present invention
  • FIG. 3 depicts an end view of the lands of FIG. 1;
  • FIG. 4 depicts a side view of the lands of FIG. 1;
  • FIG. 5 is a graphical comparison of the cross-directional strength of a thermal bonded fabric formed of a first fiber according to a prior art patterned calender roll and the patterned calender roll of the present invention
  • FIG. 6 is a graphical comparison of the cross-directional elongation of the fabrics formed from the first fiber
  • FIG. 7 is a graphical comparison of the cross-directional strength of a thermal bonded fabric formed of a second fiber according to a prior art patterned calender roll and the patterned calender roll of the present invention
  • FIG. 8 is a graphical comparison of the cross-directional elongation of the fabrics formed from the second fiber
  • FIG. 9 is a graphical comparison of the cross-directional strength of a thermal bonded fabric formed of a third fiber according to a prior art patterned calender roll and the patterned calender roll of the present invention.
  • FIG. 10 is a graphical comparison of the cross-directional elongation of the fabrics formed by the third fiber.
  • FIG. 11 is a schematic depiction of bonding regions of a calender roll according to the present invention.
  • FIG. 12 is a schematic depiction of the land pattern of a prior art calender roll.
  • the present invention is directed to method and apparatus for thermal bonding high elongation nonwoven fabric, as well as the nonwoven fabric produced thereby, and articles including such nonwoven fabric.
  • the nonwoven fabric of the instant invention is composed of various forms of fibers, and within the scope of the present invention, include filaments and staple fibers. These terms are used in their ordinary commercial meanings. Typically, “filament” is used herein to refer to the continuous fiber on the spinning machine. “Staple fiber” is used to refer to cut fibers or filaments. Staple fiber is used in a multitude of products, such as personal hygiene, medical, industrial and automotive products and commonly ranges in length from about 5 mm to about 16 cm. Preferably, for instance, staple fibers for nonwoven fabrics useful in diapers have lengths about 2.5 cm to 7.6 cm, more preferably about 3.2 cm to 5 cm. Thicknesses of fiber or filament are measured in denier per filament (dpf), which is the weight in grams of 9,000 m (9 km) of filament. As a matter of convenience, “fiber” is herein also used to describe filament or staple fiber.
  • dpf denier per filament
  • the calender roll according to the present invention is constructed and arranged to provide a lower degree of bonding area than usual as well as fewer bonding points on individual fibers.
  • the lands are dimensioned and positioned on the calender roll to be sufficiently spaced apart such that there are a minimum number of fibers that may not be bonded.
  • the lands are spaced such that all, or substantially all, individual fibers oriented in the machine direction have bond points.
  • the lands should not be so distanced from each other that the strength properties, including machine direction strength and cross-directional strength, are rendered unacceptable.
  • the lands should be constructed and arranged to provide fibers than are capable of sliding with respect to one another to thereby provide a highly stretchable fabric, especially while providing a fabric of sufficient strength characteristics.
  • the lands in one row 29 are staggered with respect to lands in an adjacent row 30 so that there are a reduced number of bonding points, with bonding points occurring on alternating rows 29 and 31 of lands, at least for fibers oriented in the machine direction.
  • fibers extending in the machine direction, or substantially in the machine direction will only have one bonding point for each adjacent two rows, such as adjacent rows 29 and 30 , and will have two bonding points for alternating rows, such as alternating rows 29 and 31 .
  • the lands on the calender roll are preferably constructed and arranged to ensure that bonding points are present on each fiber, except for fibers 6 that are oriented at an angle of greater than about 15° with respect to the machine direction, more preferably about 35° to 55°, with a preferred value being about 45°, with respect to the machine direction, and within the space 7 between lands, which will be a no bond region.
  • the spacing between the rows of lands (in the machine direction) can be varied, but the spacing should not be increased to the extent the angle between lands in successive rows (in the machine direction) exceeds an angle of greater than about 15° with respect to the machine direction, more preferably about 35° to 55°, and most preferably an angle of about 45°.
  • angles of about 35° to 55°, as well as 45° is being made primarily to assist an understanding of the spacing of the lands.
  • the likelihood that a fiber would be positioned at only about a 45° angle is practically zero.
  • at least a major number of the fibers, and substantially all fibers will be oriented in the machine direction.
  • fibers will not ordinarily align in a linear configuration.
  • bonding points will be present on substantially every fiber, except for fibers that are oriented at an angle of greater than about 15° with respect to the machine direction, more preferably about 35° to 55°, and preferably about 45°, with respect to the machine direction, and within the space 7 between lands, or fibers that are aligned substantially at an angle of 90° with respect to the machine direction, as illustrated at region 8 , which also will not have bonding points.
  • This will result in a fabric having fibers with a reduced number of bond points, thereby providing a highly stretchable fabric, especially while providing a fabric of sufficient strength characteristics.
  • the lands on the calender roll are constructed and arranged to provide a bond area which is in the range of about 5% to 20%, more preferably about 8% to 15%, even more preferably about 8% to 12%, with a particularly preferred bond area being about 11%.
  • the fibers can be processed on high speed machines for the making of various materials, in particular, nonwoven fabrics that can have diverse uses, including cover sheets, acquisition layers and back sheets in diapers.
  • the fibers of the present invention enable the production of nonwoven materials at speeds as high as about 500 ft/min, more preferably as high as about 700 to 800 ft/min, and even as more preferably as high as about 980 ft/min (about 300 meters/min) or higher, such as about 350 meters/min, at basis weights from about 10 g/yd 2 (gsy) to 50 gsy, more preferably 20-40 gsy, and having cross-directional strengths, for a basis weight of about 20 gsy, on the order of at least about 200 g/in, more preferably 300 to 400 g/in, preferably greater than about 400 g/in, and more preferably as high as about 650 g/in, or higher.
  • the fabrics can have an elongation of about at least about 120%, more preferably at least about 140%, even more preferably at least about 160%, even more preferably at least about 180%, even more preferably at least about 200%, even more preferably at least about 250%, and even more preferably at least about 300%, and a toughness of about 600 to 2100 g/in, preferably about 1440-2100 g/in.
  • a portion of a calender roll 1 is depicted illustrating a plurality of lands 2 that are configured to have a generally truncated pyramidal shape, and are arranged in parallel rows with the lands 2 in alternating rows being staggered.
  • the calender roll 1 is formed as a cylindrical member which may have a diameter in the range of about 30 cm to 180 cm, preferably about 45 cm to 90 cm, and a face width in the range of about 45 cm to 450 cm, preferably about 50 cm to 400 cm, which includes the pattern of staggered lands 2 as shown in FIG. 1, such as by embossing, engraving, or by any method for forming lands on a calender rolls.
  • the upper surface 3 of each land preferably has a rectangular or substantially rectangular shape as shown, but can have other shapes as long as bonding spots can be attained.
  • the width 9 of upper surface 3 aligned in the circumferential or machine direction (FIG. 1, arrow A) of the calender roll is in the range of about 0.036 cm to 0.066 cm, and preferably about 0.043 cm to 0.059 cm, with a preferred value being about 0.051 cm.
  • the length 10 of the upper surface 3 aligned in the cross-direction (FIG. 1, arrow B) of the calender roll is about 0.071 cm to 0.133 cm, and preferably about 0.087 cm to 0.117 cm, with a preferred value being about 0.102 cm.
  • the base 4 of each land preferably has a rectangular or substantially rectangular shape as shown, but can have other shapes as long as bonding spots can be attained.
  • the width 11 of the base 4 aligned in the circumferential or machine direction of the calender roll is in the range of about 0.075 cm to 0.139 cm, and preferably about 0.091 cm to 0.123 cm, with a preferred value being about 0.107 cm.
  • the length 12 of base 4 aligned in the cross-direction of the calender roll is in the range of about 0.111 cm to 0.205 cm, preferably about 0.134 cm to 0.182 cm, with a preferred value being about 0.158 cm,
  • the lands have a height 13 of about 0.053 cm to 0.099 cm, and preferably about 0.065 cm to 0.087 cm, with a preferred value being about 0.076 cm.
  • Side walls 5 have a taper ⁇ (as shown in FIGS. 3 and 4) in the range of about 14° to 35°, more preferably 14° to 26°, even more preferably about 17° to 23°, with a preferred value being about 20°.
  • the centers of adjacent lands in a row are spaced apart a distance 14 in the range of about 0.142 cm to 0.264 cm, and preferably about 0.173 cm to 0.233 cm, with a preferred value being about 0.203 cm apart.
  • the centers of lands in adjacent rows are spaced apart a distance 15 in the range of about 0.071 cm to 0.133 cm, and preferably about 0.087 cm to 0.117 cm, with a preferred value being about 0.102 cm apart.
  • the bases 4 are preferably constructed and arranged such that they overlap.
  • the upper surface or central land area 3 of each land in a row is dimensioned and positioned so as not to overlap with the upper surface or central land area 3 of lands in an adjacent row.
  • the base 4 of lands in one row will preferably overlap with bases 4 in an adjacent row.
  • bases 4 positioned within a row will overlap with two bases 4 in an adjacent row, whereas bases 4 positioned at the end of a row will usually overlap only one base 4 in an adjacent row.
  • the centers of the lands between adjacent rows are spaced apart a distance 16 in the range of about 0.157 cm to 0.291 cm, and preferably about 0.190 cm to 0.258 cm, with a preferred value being about 0.224 cm.
  • the calender roll according to the present invention can be constructed with various materials, such as steel including ANSI 1030 or better engravable steel. Moreover, the lands can be formed in any manner, such as by etching.
  • the above-described patterned calender roll is utilizable in the method of the present invention which includes thermally bonding fibers together to form a nonwoven fabric utilizing the calendar roll to form bond spots in the nonwoven fabric.
  • heat and pressure can be applied to the web in the nip between the calender roll of the present invention and a smooth roll for thermally bonding the fibers with a pattern of lands that form bonding points.
  • portions of the fiber are fused or melted together to form the bond points.
  • the pressure and temperature will vary with the material of the web to be bonded. The temperature can range over a wide range of temperatures, such as from about 110° C. to 220° C.
  • the rolls are heated to a temperature of about 135° C. to 200° C., more preferably about 140° C. to 185° C., and even more preferably about 140° C. to 180° C., and apply a pressure of about 160 to 480 pounds per linear inch, more preferably about 180 to 300 pounds per linear inch, with a preferred valued being about 240 pounds per linear inch.
  • the bond points and non-bonded areas contribute to the strength of the nonwoven material, as well as its softness, stretchability, and elongation properties.
  • the fibers useful in accordance with the present invention can comprise various polymers.
  • polymers useful with the present invention can comprise various spinnable polymeric materials such as polyolefins and blends comprising polyolefins.
  • the polymer is a polypropylene or a blend comprising a polypropylene.
  • the polypropylene can comprise any polypropylene that is spinnable.
  • the polypropylene can to be atactic, heterotactic, syndiotactic, isotactic and stereoblock polypropylene—including partially and fully isotactic, or at least substantially fully isotactic—polypropylenes.
  • Polypropylenes which may be spun in the inventive system can be produced by any process.
  • the polypropylene can be prepared using Zeigler-Natta catalyst systems, or using homogeneous or heterogeneous metallocene catalyst systems.
  • polymers include homopolymers, various polymers, such as copolymers and terpolymers, and mixtures (including blends and alloys produced by mixing separate batches or forming a blend in situ).
  • copolymer is understood to include polymers of two monomers, or two or more monomers, including terpolymers.
  • the polymer can comprise copolymers of olefins, such as propylene, and these copolymers can contain various components.
  • such copolymers can include up to about 20 weight %, and, even more preferably, from about 0 to 10 weight % of at least one of ethylene and butene.
  • varying amounts of these components can be contained in the copolymer depending upon the desired fiber.
  • the polypropylene can comprise dry polymer pellet, flake or grain polymers having a narrow molecular weight distribution or a broad molecular weight distribution, with a broad molecular weight distribution being preferred.
  • the term “broad molecular weight distribution” is here defined as dry polymer pellet, flake or grain preferably having an MWD value (i.e., Wt.Av.Mol.Wt./No.Av.Mol.Wt. measured by SEC as discussed below) of at least about 5, preferably at least about 5.5, more preferably at least about 6.
  • the MWD is typically about 2 to 15, more typically, less than about 10.
  • the resulting spun melt preferably has a weight average molecular weight varying from about 3 ⁇ 10 5 to about 5 ⁇ 10 5 , a broad SEC molecular weight distribution generally in the range of about 6-20 or above, a spun melt flow rate, MFR, (determined according to ASTM D-1238-86 (condition L;230/2.16), which is incorporated by reference herein in its entirety) of about 13 to about 50 g/10 minutes, and/or a spin temperature conveniently within the range of about 220°-315° C., preferably about 300° C.
  • the polypropylene can be linear or branched, such as disclosed by U.S. Pat. No. 4,626,467 to Hostetter, which is incorporated by reference herein in its entirety, and is preferably linear.
  • the polypropylene to be made into fibers can include polypropylene compositions as taught in Gupta et al. U.S. Pat. No. 5,629,080, and European Patent Application No. 0 552 013 to Gupta et al., which are incorporated by reference herein in their entireties.
  • polymer blends such as disclosed in Kozulla, U.S. Pat. application Ser. No. 08/358,884, filed Dec.
  • the production of polymer fibers for nonwoven materials usually involves the use of a mix of at least one polymer with nominal amounts of additives, such as antioxidants, stabilizers, pigments, antacids, process aids and the like.
  • the polymer or polymer blend can include various additives, such as melt stabilizers, antioxidants, pigments, antacids and process aids.
  • additives such as antioxidants, stabilizers, pigments, antacids and process aids.
  • the types, identities and amounts of additives can be determined by those f ordinary skill in the art upon consideration of requirements of the product.
  • preferred antioxidants include Irganox 1076, and Irgafos 168 (both from Ciba-Geigy, Tarrytown, N.Y.) which may typically be present in the polymer composition in amounts of about 50-150 ppm (Irganox 1076) or about 200-1000 ppm (Irgafos 168) based on the weight of the total composition.
  • Various finishes can be applied to the filaments to maintain or render them hydrophilic or hydrophobic.
  • one or more components can be included in the polymer blend for modifying the surface properties of the fiber, such as to provide the fiber with repeat wettability, or to prevent or reduce build-up of static electricity.
  • Hydrophobic finish compositions preferably include antistatic agents.
  • Hydrophilic finishes may also include such agents.
  • Preferable hydrophobic finishes include those of U.S. Pat. No. 4,938,832, European Patent Application No. 486,158, all to Schmalz, which are incorporated by reference as if set forth in their entireties herein. These documents describe fiber finish compositions containing at least one neutralized phosphoric acid ester having a lower alkyl group, such as a 1-8 carbon alkyl group, which functions as an antistat, in combination with polysiloxane lubricants.
  • hydrophobic finish composition that can be used with the present invention is disclosed in U.S. Pat. No. 5,403,426, to Johnson et al., incorporated by reference as if set forth in its entirety herein.
  • This patent describes a method of preparing hydrophobic fiber for processing inclusive of crimping, cutting, carding, compiling and bonding.
  • the surface modifier comprises one or more of a class of water soluble compounds substantially free of lipophilic end groups and of low or limited surfactant properties.
  • hydrophobic finish composition that can be used with the present invention is disclosed in U.S. patent application Ser. No. 08/728,490, filed Oct. 9, 1996, to Hirwe et al. and WO 98/15685, which are incorporated by reference as if set forth in their entirety herein.
  • the hydrophobic finish compositions of these documents comprise hydrophobic esters of pentaerythritol homologs, preferably hydrophobic esters of pentaerythritol and pentaerythritol oligomers. Finish compositions comprising such a lubricant may further comprise other lubricants, anti-static agents, and/or other additives.
  • U.S. Pat. No. 5,540,953, to Harrington incorporated by reference as if set forth in its entirety herein, describes antistatic compositions useful in the preparation of hydrophobic fibers and nonwoven fabrics.
  • One finish described therein comprises 1) at least one neutralized C 3 -C 12 alkyl or alkenyl phosphate alkali metal or alkali earth metal salt, and 2) a solubilizer.
  • a second finish described therein comprises at least one neutralized phosphoric ester salt.
  • ingredients that may comprise a finish composition useful with the present invention include emulsifiers or other stabilizers, and preservatives such as biocides.
  • emulsifiers or other stabilizers include emulsifiers or other stabilizers, and preservatives such as biocides.
  • One preferred biocide is Nuosept® 95, 95% hemiacetals in water, available from Nuodex Inc. division of HULS America Inc. (Piscataway, N.J.).
  • Finish compositions comprising hydrophilic finishes or other hydrophobic finishes, may be selected by those of ordinary skill in the art according to the characteristics of the apparatus and the needs of the product being manufactured.
  • Other additives such as antistatic agents, stabilizers, emulsifiers and preservatives may be similarly selected.
  • the fibers are preferably polypropylene fibers, and more preferably are polypropylene fibers formed as skin-core fibers.
  • Fibers without a skin-core structure can be prepared by providing conditions which result in the manufacture of fibers without a skin-core structure. Such conditions may be achieved, for example, by providing an environment that sufficiently avoids oxidation of the surface of the filaments.
  • Fibers with a skin-core structure can be produced by any procedure that achieves oxidation, degradation and/or lowering of molecular weight of the polymer blend at the surface of the fiber as compared to the polymer blend in an inner core of the fiber.
  • a skin-core structure can be obtained, for example, through a delayed quench and exposure to an oxidative environment, as disclosed in U.S. Pat. Nos. 5,431,994, 5,318,735 and 5,281,378, all to Kozulla, and European Application No. 719 879 A2, all of which are incorporated above by reference.
  • Another method of obtaining a skin-core structure involves employing a heated spinnerette to achieve thermal degradation of the filament surface, as disclosed in U.S. Pat. No.
  • the skin-core structure can comprise a skin showing an enrichment of ruthenium staining of at least about 0.2 ⁇ m, more preferably at least about 0.5 ⁇ m, more preferably at least about 0.7 ⁇ m, even more preferably at least about 1 ⁇ m, and even more preferably at least about 1.5 ⁇ m.
  • the skin thickness can also be stated in terms of enrichment in staining of the equivalent diameter of the fiber.
  • the enrichment in ruthenium. staining can comprise at least about 1% and up to about 25% of the equivalent diameter of the fiber, preferably about 2% to 10% of the equivalent diameter of the fiber.
  • the skin-core structure of the instant invention can be determined using a hot stage test, as disclosed in U.S. Pat. No. 5,705,119 to Takeuchi which is incorporated by reference herein, and a skin-core structure is present when a residue trail is present.
  • the skin-core structure comprises chemical modification of a filament to obtain the skin-core structure, and does not comprise separate components being joined along an axially extending interface, such as in sheath-core and side-by-side bicomponent fibers.
  • the skin-core structure can be utilized in a composite fiber, such as the skin-core structure being present in the sheath of a sheath-core fiber in the manner disclosed in U.S. Pat. Nos. 5,281,378, 5,318,735 and 5,431,994 and EP Application No. 719 879 A2, which were discussed above and incorporated herein.
  • skin-core fibers can be prepared by providing conditions in any manner so that during extrusion of the polymer blend a skin-core structure is formed.
  • a hot extrudate such as an extrudate exiting a spinnerette
  • This elevated temperature can be achieved using a number of techniques, such as disclosed in the above discussed patents to Kozulla, and in U.S. and foreign applications to Takeuchi et al., discussed above and incorporated herein.
  • skin-core filaments can be prepared in the inventive system through the method of U.S. Pat. Nos. 5,281,378, 5,318,735 and 5,431,994 to Kozulla, and European Patent Application No. 719 879 A2 in which the temperature of the hot extrudate can be provided above at least about 250° C. in an oxidative atmosphere for a period of time sufficient to obtain the oxidative chain scission degradation of its surface.
  • This providing of the temperature can be obtained by delaying cooling of the hot extrudate as it exits the spinnerette, such as by blocking the flow of a quench gas reaching the hot extrudate.
  • Such blocking can be achieved by the use of a shroud or a recessed spinnerette that is constructed and arranged to provide the maintaining of temperature.
  • the skin-core structure can be obtained by heating the polymer blend in the vicinity of the spinnerette, either by directly heating the spinnerette or an area adjacent to the spinnerette.
  • the polymer blend can be heated at a location at or adjacent to the at least one spinnerette, by directly heating the spinnerette or an element such as a heated plate positioned approximately 1 to 4 mm above the spinnerette, so as to heat the polymer composition to a sufficient temperature to obtain a skin-core fiber structure upon cooling, such as being immediately quenched, in an oxidative atmosphere.
  • the extrusion temperature of the polymer may be about 230° C. to 250° C.
  • the spinnerette may have a temperature at its lower surface of preferably at least about 250° C. across the exit of the spinnerette in order to obtain oxidative chain scission degradation of the molten filaments to thereby obtain filaments having a skin-core structure.
  • skin-core fibers prepared in the inventive system are not limited to those obtained by the above-described techniques. Any technique that provides a skin-core structure to the fiber is included in the scope of this invention.
  • a ruthenium staining test is utilized.
  • the substantially non-uniform morphological structure of the skin-core fibers according to the present invention can be characterized by transmission electron microscopy (TEM) of ruthenium tetroxide (RuO 4 )-stained fiber thin sections.
  • TEM transmission electron microscopy
  • RuO 4 ruthenium tetroxide
  • samples of fibers are stained with aqueous RuO 4 , such as a 0.5% (by weight) aqueous solution of ruthenium tetroxide obtainable from Polysciences, Inc., overnight at room temperature.
  • aqueous RuO 4 such as a 0.5% (by weight) aqueous solution of ruthenium tetroxide obtainable from Polysciences, Inc.
  • Stained fibers are embedded in Spurr epoxy resin and cured overnight at 60° C.
  • the embedded stained fibers are then thin sectioned on an ultramicrotome using a diamond knife at room temperature to obtain microtomed sections approximately 80 nm thick, which can be examined on conventional apparatus, such as a Zeiss EM-10 TEM, at 100 kV.
  • Energy dispersive x-ray analysis (EDX) was utilized to confirm that the RuO 4 had penetrated completely to the center of the fiber.
  • the ruthenium staining test would be performed to determine whether a skin-core structure is present in a fiber. More specifically, a fiber can be subjected to ruthenium staining, and the enrichment of ruthenium (Ru residue) at the outer surface region of the fiber cross-section would be determnined. If the fiber shows an enrichment in the ruthenium staining for a thickness of at least about 0.2 ⁇ m or at least about 1% of the equivalent diameter for fibers having a denier of less than 2, the fiber has a skin-core structure.
  • the ruthenium staining test is an excellent test for determining skin-core structure, there may be certain instances wherein enrichment in ruthenium staining may not occur. For example, there may be certain components within the fiber that would interfere with or prevent the ruthenium from showing an enrichment at the skin of the fiber, when, in fact, the fiber comprises a skin-core structure.
  • the description of the ruthenium staining test herein is in the absence of any materials and/or components that would prevent, interfere with, or reduce the staining, whether these materials are in the fiber as a normal component of the fiber, such as being included therein as a component of the processed fiber, or whether these materials are in the fiber to prevent, interfere with or reduce ruthenium staining.
  • the present invention utilizes nonwoven materials including the fibers described above which are thermally bonded together.
  • nonwoven materials including the fibers described above which are thermally bonded together.
  • the resulting nonwoven materials possess exceptional cross-directional strength, softness and elongation properties.
  • These nonwoven materials can be used as at least one layer in various products, including hygienic products, such as sanitary napkins, incontinence products and diapers, comprising at least one liquid absorbent layer and at least one nonwoven material layer of the present invention and/or incorporating fibers of the present invention thermally bonded together.
  • the articles according to the present invention can include at least one liquid permeable or impermeable layer.
  • a diaper incorporating a nonwoven fabric of the present invention would include, as one embodiment, an outermost impermeable or permeable layer, an inner layer of the nonwoven material, and at least one intermediate absorbent layer.
  • an outermost impermeable or permeable layer an inner layer of the nonwoven material
  • at least one intermediate absorbent layer a plurality of nonwoven material layers and absorbent layers can be incorporated in the diaper (or other hygienic product) in various orientations, and a plurality of outer permeable and/or impermeable layers can be included for strength considerations.
  • nonwovens of the present invention can include a plurality of layers, with the layers being of the same fibers or different. Further, not all of the layers need include skin-core fibers of the polymer blend described above.
  • the nonwovens of the present invention can be used by themselves or in combination with other nonwovens, or in combination with other nonwovens or films.
  • suitable fibers are the following which are skin-core polypropylene fibers available from Hercules Incorporated, a Delaware corporation: T190 fiber which is a 2.2 dpf (denier-per-filament) staple fiber; T194 fiber which is a 2.6 dpf staple fiber; and T198 fiber which is a 2.6 dpf staple fiber.
  • the web may be a carded fibrous web or formed from continuous filaments and microfiber network structures, or from any of the many known conventional methods.
  • the fibers can be formed in accordance with the process disclosed in co-pending U.S. application Ser. No. 08/728,491, filed Oct. 9, 1996, and WO 97/37065, the entire disclosures of which are expressly incorporated herein by reference.
  • the fibers of the present invention can have any cross-sectional configuration, such as oval, circular, diamond, delta, trilobal—“Y”-shaped, “X”-shaped, and concave delta, wherein the sides of the delta are slightly concave.
  • the fibers include a circular or a concave delta cross-section configuration.
  • the cross-sectional shapes are not limited to these examples, and can include other cross-sectional shapes.
  • the fibers can include hollow portions, such as a hollow fiber, which can be produced, for example, with a “C” cross-section spinnerette.
  • normalized cross-directional strength and elongation were determined using test strips (six per sample) of each nonwoven, 1 inch ⁇ 7 inches (25 mm ⁇ 178 mm) using a tensile tester Model 1122 from Instron Corporation, Canton, Mass. Specifically, the breaking load and elongation are determined in accordance with the “cut strip test” in ASTM D-1682-64 (Re-approved 1975), which is incorporated by reference in its entirety, using the Instron Tester set at constant rate of traverse testing mode. The gauge length is 12.7 cm, the crosshead speed is 12.7 cm/minute, and the extension rate is 100%/minute.
  • Nonwoven fabrics were prepared by carding the fibers into conventional fiber webs at 250 feet per minute (76 m/min) using equipment and procedures as discussed in Legare, R. J., 1986 TAPPI Synthetic Fibers for Wet System and Thermal Bonding Applications, Boston Park Plaza Hotel & Towers, Boston, Mass. Oct. 9-10, 1986, “Thermal Bonding of Polypropylene Fibers in Nonwovens”, pages 1-13, 57-71 and attached Tables and Figures.
  • the Webmaster® randomizers described in the TAPPI article were not used. This article is incorporated herein in its entirety, by reference thereto.
  • Two layers of the carded staple fibers were stacked in the machine direction, and bonded using either a calender roll according to the present invention (identified as Roll B in Tables I-III), and a known diamond design embossed calender roll (identified as Roll A in Tables I-III) and a smooth roll at roll temperatures ranging from about 145 to 170° C. and roll pressures of 420 Newtons per linear centimeter (240 pounds per linear inch) to obtain nonwovens weighing nominally about 23.9 grams per square meter (20 ⁇ 1 grams per square yard).
  • a calender roll according to the present invention identified as Roll B in Tables I-III
  • a known diamond design embossed calender roll identified as Roll A in Tables I-III
  • a smooth roll at roll temperatures ranging from about 145 to 170° C. and roll pressures of 420 Newtons per linear centimeter (240 pounds per linear inch) to obtain nonwovens weighing nominally about 23.9 grams per square meter (20 ⁇ 1 grams per square yard).
  • the diamond pattern calender roll had a 15% land area, 58.8 spots/sq.cm. with a depth of 0.076 cm. Further, the diamonds had a width (w) of 0.101 cm, a height (h) of 0.051 cm, and are spaced height-wise (H) 0.22 cm on center, and width-wise (L) 0.152 cm on center, as illustrated in FIG. 12 .
  • the calender roll configured in accordance with the present invention (Roll B) was formed of ANSI 1030 engravable steel which was engraved to provide a plurality of lands, and ground in a cylindrical grinder to provide a minimum loss of outer diameter of the roll while keeping the roll concentric. Next the roll was polished to deburr and finished to 4-6 RMS. The resulting roll had a nominal diameter of approximately 24.65 cm and a length of about 57.15 cm, and the outer cylindrical surface included a plurality of lands having a truncated pyramidal shape, with a land or bond area of approximately 11% and 22 spots/sq.cm.
  • each truncated pyramidal shaped land had a rectangular base having a short side width (aligned in the machine or radial direction of the roll) of 0.107 cm, a long side length (aligned in the cross or longitudinal direction of the roll) of 0.158 cm, and a height of 0.76 cm.
  • the upper surface of each land had short sides of 0.51 cm that extend parallel to the width of the base and had long sides of 0.102 cm that extend parallel to the length of the base.
  • the sides of the lands tapered from the base to the upper surface at an angle of 20°.
  • the lands were provided on the outer peripheral surface and arranged in rows parallel to the longitudinal axis of the roll, and included 178 rows of 263 lands (short rows) alternating with 179 rows of 274 lands (long rows), respectively.
  • the centers of the endmost lands in the short rows were spaced 2.007 cm from the roll ends, while the centers of the endmost lands in the long rows were spaced 0.244 cm from the roll ends.
  • the centers of the lands of adjacent rows were spaced apart a distance of 0.224 cm (in the radial direction) and the distance from the center of a land in one row to the center of a land in an adjacent row (in the longitudinal direction of the roll) was 0.102 cm. Also, the distance between the bases in adjacent rows (in the radial direction) was 0.117 cm while the distance between bases in adjacent rows (in the longitudinal direction) was 0.046 cm.
  • Tables I-III compare the cross-directional strength (CDS) and cross-directional elongation (CDE) of fabrics formed of three different fibers, with each table comparing a fabric formed with a conventional patterned roll (Roll A) and with a patterned roll according to the present invention (Roll B). As shown in Table 1 for a T190 fiber with 2.2 DPF, and as depicted in FIGS.
  • the cross-directional strength for a fabric formed from a calender roll according to the present invention is somewhat less than that formed by the conventional calender roll (curve 18 ).
  • the cross-directional elongation of the fabric formed in accordance with the present invention has greatly increased elongation as compared to that formed by the conventional calender roll (curve 20 ).
  • Table II data which is for a T198 fiber with 2.6 DPF and the Table III data which is for a T194 fiber with a 2.6 DPF, similar results can be seen when comparing the fabric formed with these fibers by the conventional calender roll A (curves 21 , 23 , 25 and 27 as depicted in FIGS. 7-10) when compared with the patterned roll B according to the present invention (curves 22 , 24 , 26 , 28 as depicted in FIGS. 7 - 10 ).

Abstract

A method of forming a thermally bonded, nonwoven polypropylene fabric is provided and includes passing a web of thermally bondable skin-core polypropylene fibers through a calender nip under heat and pressure to produce a nonwoven fabric having elongation. The patterned calender roll is embossed with a plurality of spaced and staggered lands particularly dimensioned, configured and oriented to provide the desired bonding spot size and spacing between the bonding spots such that when utilized in the calender roll, an improved soft polypropylene fabric or cover sheet having a high elongation results.

Description

BACKGROUND OF THE INVENTION
1. Field of the Invention
The present invention relates to thermal bonding of nonwoven fabric, especially high elongation nonwoven fabric, and to calender rolls for producing such nonwoven fabric as well as to nonwoven fabrics and articles including nonwoven fabrics.
2. Description of Background Information
Nonwoven fabrics are typically made by making a web, and then thermally bonding the fibers together. For example, staple fibers can be converted into nonwoven fabrics using, for example, a carding machine, and the carded fabric can be thermally bonded. The thermal bonding can be achieved using various heating techniques, including heating with heated rollers, hot air and heating through the use of ultrasonic welding.
When heated rollers are utilized to bond the carded fabric, typically there is utilized one roll that is smooth and a calender roll that includes bonding spots thereon. The material to be thermally bonded is fed through a nip between the smooth roll and the calendar roll, with sufficient heat being applied to obtain thermal bonding of the material.
Conventional thermal bonding calender rolls, such as embossed calender rolls, are configured with a plurality of lands to provide bonding spots to provide maximum machine direction strength and cross direction strength, while preferably providing a soft feel or touch to the material, especially when forming the thermal bonded material or fabric from synthetic materials. Such thermal bonded fabric is often used to form nonwoven cover stock, which is typically used for hygiene products, such as a top sheet of a diaper. In such applications, one face or side of the cover stock material is placed in contact with a human body, for example, placed on the skin of a baby. Therefore, it is desirable that the face in contact with the human body exhibit softness.
The conventional processes utilize embossed thermal bonding calender rolls designed with a plurality of spaced lands that form bonding spots to provide a soft touch, as well as maximum machine direction and cross-direction strength. However, most of the prior art card-produced nonwoven fabrics do not have acceptable stretch characteristics.
There is therefore a need to produce nonwoven fabric having a high degree of elongation, especially with acceptable strength.
SUMMARY OF THE INVENTION
Accordingly, it is an object of the present invention to provide improved methods of manufacturing thermal bonded, nonwoven, fibrous web materials of high elongation, preferably with acceptable strength.
It is also an object of the present invention to provide a thermal bonding calender roll that will produce thermally bonded nonwoven material with high stretch or elongation.
The present invention provides a method of manufacturing thermally bonded fabric having high elongation, comprising forming a web of thermally bondable polypropylene fibers; passing the web over a heated calender roll having a patterned surface including a plurality of rows of lands, with each of the lands having an upper surface, with upper surfaces of lands in adjacent rows being staggered such that they do not overlap one another in a machine direction; and thermally bonding the fibers at bond points located about the upper surfaces of the lands such that fibers extending substantially in the machine direction will only have one bond point for adjacent rows.
The polypropylene fibers are preferably skin core polypropylene fibers.
The web can be provided as a carded fibrous web, or as a plurality of continuous filaments.
The elongation of the nonwoven fabric is at least about 120%, preferably greater than about 140%, more preferably greater than about 160%, even more preferably greater than about 180%, even more preferably greater than about 200%, even more preferably greater than about 250%, and most preferably greater than 300%.
The passing of the web over a heated calender roll can comprise passing the fibrous web between a pair of cooperating rolls in a calender nip, at least one of the pair of rolls having the patterned surface and comprising a cylindrical roll having an outer cylindrical surface including a plurality of lands; the lands being arranged on the outer cylindrical surface in a plurality of spaced apart rows; each of the lands comprising a tapered shape including a base, preferably substantially rectangular, tapering to an upper surface, which is preferably substantially rectangular; the upper surface including short sides oriented in the machine direction of about 0.036 cm to 0.066 cm in length, preferably about 0.043 cm to 0.059 cm, with a preferred value being about 0.051 cm, and long sides of about 0.071 cm to 0.133 cm in length oriented in a cross direction, preferably about 0.087 cm to 0.117 cm, with a preferred value being about 0.102 cm; adjacent rows of the lands being spaced apart a distance, with respect to the centers of the lands, of about 0.157 cm to 0.291 cm, preferably about 0.190 cm to 0.258 cm, with a preferred value being about 0.224; upper surfaces of lands in adjacent rows being staggered such that upper surfaces in adjacent rows do not overlap with one another in a machine direction providing a plurality of spaced apart bond points capable of bonding fibers extending substantially in the machine direction at only one bond point for adjacent rows; and the plurality of lands providing a bond area up to about 20%, preferably from about 5% to 20%, more preferably about 8% to 15%, even more preferably about 8% to 12%, with a preferred value being about 11%
The upper surfaces of the lands can be substantially rectangular. Moreover, the bases can overlap in the machine direction in adjacent rows.
Centers of the lands in each row are spaced apart by a distance of about 0.142 cm to 0.264 cm, preferably about 0.173 cm to 0.233 cm, with a preferred value being about 0.203 cm, and centers of the lands in adjacent rows are spaced apart by a distance of about 0.071 cm to 0.133 cm, preferably about 0.087 cm to 0.117 cm, with a preferred value being about 0.102 cm. The lands are constructed and arranged such that a straight fiber lying at an angle of greater than 15% with respect to the machine direction, more preferably about 35° to 55°, and even more preferably 45°, is positioned in a space between the lands, whereby the fiber is not be bonded.
The lands are preferably of a truncated pyramidal shape, preferably having substantially rectangular bases with short sides about 0.075 cm to 0.139 cm in length oriented in the machine direction, preferably 0.091 cm to 0.123 cm, with a preferred value being about 0.107 cm, and long sides about 0.111 cm to 0.205 cm in length oriented in the cross direction, preferably about 0.134 cm to 0.182 cm, with a preferred value being about 0.158 cm, and tapered side walls extending between the base and the upper surface at an angle a of about 14° to 35°, preferably about 17° to 26°, more preferably about 17° to 23°, with a preferred value being about 20°.
The lands can have a height of about 0.053 cm to 0.099 cm, preferably about 0.065 cm to 0.087 cm, with a preferred value being about 0.076 cm.
There is also provided a method of manufacturing thermally bonded fabric having high elongation, comprising forming a web comprising thermally bondable skin-core polypropylene fibers; passing the web over a calender roll having a patterned surface including a plurality of rows of lands, with each of the lands having an upper surface, with upper surfaces of lands in adjacent rows being staggered such that they do not overlap one another in a machine direction; applying heat and pressure to the fibrous web at a location of the calender roll to thermally bond the fibers at bond points located about the upper surfaces of the lands such that fibers extending substantially in the machine direction will only have one bond point for adjacent rows.
The present invention is also directed to the calender roll and to polypropylene fabrics formed by the methods.
BRIEF DESCRIPTION OF THE DRAWINGS
The above and other features and advantages of the present invention will be made apparent from the following description of the preferred embodiments, given as non-limiting examples, with reference to the accompanying drawings, in which:
FIG. 1 depicts a portion of the patterned calender roll according to the present invention, with the pattern broken away at the central portion;
FIG. 2 depicts the relative spacing of the lands forming the bond spots according to the present invention;
FIG. 3 depicts an end view of the lands of FIG. 1;
FIG. 4 depicts a side view of the lands of FIG. 1;
FIG. 5 is a graphical comparison of the cross-directional strength of a thermal bonded fabric formed of a first fiber according to a prior art patterned calender roll and the patterned calender roll of the present invention;
FIG. 6 is a graphical comparison of the cross-directional elongation of the fabrics formed from the first fiber;
FIG. 7 is a graphical comparison of the cross-directional strength of a thermal bonded fabric formed of a second fiber according to a prior art patterned calender roll and the patterned calender roll of the present invention;
FIG. 8 is a graphical comparison of the cross-directional elongation of the fabrics formed from the second fiber;
FIG. 9 is a graphical comparison of the cross-directional strength of a thermal bonded fabric formed of a third fiber according to a prior art patterned calender roll and the patterned calender roll of the present invention; and
FIG. 10 is a graphical comparison of the cross-directional elongation of the fabrics formed by the third fiber.
FIG. 11 is a schematic depiction of bonding regions of a calender roll according to the present invention.
FIG. 12 is a schematic depiction of the land pattern of a prior art calender roll.
DETAILED DESCRIPTION OF THE PREFERRED EMBODIMENT
The present invention is directed to method and apparatus for thermal bonding high elongation nonwoven fabric, as well as the nonwoven fabric produced thereby, and articles including such nonwoven fabric.
The nonwoven fabric of the instant invention is composed of various forms of fibers, and within the scope of the present invention, include filaments and staple fibers. These terms are used in their ordinary commercial meanings. Typically, “filament” is used herein to refer to the continuous fiber on the spinning machine. “Staple fiber” is used to refer to cut fibers or filaments. Staple fiber is used in a multitude of products, such as personal hygiene, medical, industrial and automotive products and commonly ranges in length from about 5 mm to about 16 cm. Preferably, for instance, staple fibers for nonwoven fabrics useful in diapers have lengths about 2.5 cm to 7.6 cm, more preferably about 3.2 cm to 5 cm. Thicknesses of fiber or filament are measured in denier per filament (dpf), which is the weight in grams of 9,000 m (9 km) of filament. As a matter of convenience, “fiber” is herein also used to describe filament or staple fiber.
The calender roll according to the present invention is constructed and arranged to provide a lower degree of bonding area than usual as well as fewer bonding points on individual fibers. In particular, the lands are dimensioned and positioned on the calender roll to be sufficiently spaced apart such that there are a minimum number of fibers that may not be bonded. Moreover, the lands are spaced such that all, or substantially all, individual fibers oriented in the machine direction have bond points. Moreover, the lands should not be so distanced from each other that the strength properties, including machine direction strength and cross-directional strength, are rendered unacceptable. The lands should be constructed and arranged to provide fibers than are capable of sliding with respect to one another to thereby provide a highly stretchable fabric, especially while providing a fabric of sufficient strength characteristics.
Moreover, as can be seen in FIG. 1, the lands in one row 29 are staggered with respect to lands in an adjacent row 30 so that there are a reduced number of bonding points, with bonding points occurring on alternating rows 29 and 31 of lands, at least for fibers oriented in the machine direction. In other words, fibers extending in the machine direction, or substantially in the machine direction, will only have one bonding point for each adjacent two rows, such as adjacent rows 29 and 30, and will have two bonding points for alternating rows, such as alternating rows 29 and 31.
Still further, with reference to FIG. 11, the lands on the calender roll are preferably constructed and arranged to ensure that bonding points are present on each fiber, except for fibers 6 that are oriented at an angle of greater than about 15° with respect to the machine direction, more preferably about 35° to 55°, with a preferred value being about 45°, with respect to the machine direction, and within the space 7 between lands, which will be a no bond region. The spacing between the rows of lands (in the machine direction) can be varied, but the spacing should not be increased to the extent the angle between lands in successive rows (in the machine direction) exceeds an angle of greater than about 15° with respect to the machine direction, more preferably about 35° to 55°, and most preferably an angle of about 45°.
It is noted that reference to angles of about 35° to 55°, as well as 45°, is being made primarily to assist an understanding of the spacing of the lands. For example, in practice, the likelihood that a fiber would be positioned at only about a 45° angle is practically zero. In this regard, it is noted that at least a major number of the fibers, and substantially all fibers, will be oriented in the machine direction. Moreover, fibers will not ordinarily align in a linear configuration. Again, as noted above, by maintaining the relationships according to the present invention, bonding points will be present on substantially every fiber, except for fibers that are oriented at an angle of greater than about 15° with respect to the machine direction, more preferably about 35° to 55°, and preferably about 45°, with respect to the machine direction, and within the space 7 between lands, or fibers that are aligned substantially at an angle of 90° with respect to the machine direction, as illustrated at region 8, which also will not have bonding points. This will result in a fabric having fibers with a reduced number of bond points, thereby providing a highly stretchable fabric, especially while providing a fabric of sufficient strength characteristics.
Still further, the lands on the calender roll are constructed and arranged to provide a bond area which is in the range of about 5% to 20%, more preferably about 8% to 15%, even more preferably about 8% to 12%, with a particularly preferred bond area being about 11%.
With the calendar rolls of the present invention, the fibers can be processed on high speed machines for the making of various materials, in particular, nonwoven fabrics that can have diverse uses, including cover sheets, acquisition layers and back sheets in diapers. The fibers of the present invention enable the production of nonwoven materials at speeds as high as about 500 ft/min, more preferably as high as about 700 to 800 ft/min, and even as more preferably as high as about 980 ft/min (about 300 meters/min) or higher, such as about 350 meters/min, at basis weights from about 10 g/yd2 (gsy) to 50 gsy, more preferably 20-40 gsy, and having cross-directional strengths, for a basis weight of about 20 gsy, on the order of at least about 200 g/in, more preferably 300 to 400 g/in, preferably greater than about 400 g/in, and more preferably as high as about 650 g/in, or higher. Further, the fabrics can have an elongation of about at least about 120%, more preferably at least about 140%, even more preferably at least about 160%, even more preferably at least about 180%, even more preferably at least about 200%, even more preferably at least about 250%, and even more preferably at least about 300%, and a toughness of about 600 to 2100 g/in, preferably about 1440-2100 g/in.
Turning to FIG. 1, a portion of a calender roll 1 is depicted illustrating a plurality of lands 2 that are configured to have a generally truncated pyramidal shape, and are arranged in parallel rows with the lands 2 in alternating rows being staggered. The calender roll 1 is formed as a cylindrical member which may have a diameter in the range of about 30 cm to 180 cm, preferably about 45 cm to 90 cm, and a face width in the range of about 45 cm to 450 cm, preferably about 50 cm to 400 cm, which includes the pattern of staggered lands 2 as shown in FIG. 1, such as by embossing, engraving, or by any method for forming lands on a calender rolls.
As shown in FIGS. 2-4, the upper surface 3 of each land preferably has a rectangular or substantially rectangular shape as shown, but can have other shapes as long as bonding spots can be attained. The width 9 of upper surface 3 aligned in the circumferential or machine direction (FIG. 1, arrow A) of the calender roll is in the range of about 0.036 cm to 0.066 cm, and preferably about 0.043 cm to 0.059 cm, with a preferred value being about 0.051 cm. The length 10 of the upper surface 3 aligned in the cross-direction (FIG. 1, arrow B) of the calender roll is about 0.071 cm to 0.133 cm, and preferably about 0.087 cm to 0.117 cm, with a preferred value being about 0.102 cm.
Also, as shown in FIGS. 2-4, the base 4 of each land preferably has a rectangular or substantially rectangular shape as shown, but can have other shapes as long as bonding spots can be attained. The width 11 of the base 4 aligned in the circumferential or machine direction of the calender roll is in the range of about 0.075 cm to 0.139 cm, and preferably about 0.091 cm to 0.123 cm, with a preferred value being about 0.107 cm. The length 12 of base 4 aligned in the cross-direction of the calender roll is in the range of about 0.111 cm to 0.205 cm, preferably about 0.134 cm to 0.182 cm, with a preferred value being about 0.158 cm,
The lands have a height 13 of about 0.053 cm to 0.099 cm, and preferably about 0.065 cm to 0.087 cm, with a preferred value being about 0.076 cm. Side walls 5 have a taper α (as shown in FIGS. 3 and 4) in the range of about 14° to 35°, more preferably 14° to 26°, even more preferably about 17° to 23°, with a preferred value being about 20°.
As shown in FIG. 2, the centers of adjacent lands in a row are spaced apart a distance 14 in the range of about 0.142 cm to 0.264 cm, and preferably about 0.173 cm to 0.233 cm, with a preferred value being about 0.203 cm apart. The centers of lands in adjacent rows are spaced apart a distance 15 in the range of about 0.071 cm to 0.133 cm, and preferably about 0.087 cm to 0.117 cm, with a preferred value being about 0.102 cm apart. This results in an arrangement of the lands, as seen in FIG. 2, and the lands should be constructed and arranged whereby the upper surface 3 of the lands in adjacent, such as rows 29 and 30, and in the machine direction do not overlap. Moreover, the bases 4 are preferably constructed and arranged such that they overlap.
Expanding upon the above, the upper surface or central land area 3 of each land in a row, as can be seen in FIGS. 1 and 2, is dimensioned and positioned so as not to overlap with the upper surface or central land area 3 of lands in an adjacent row. However, as can also be seen in FIGS. 1 and 2, the base 4 of lands in one row will preferably overlap with bases 4 in an adjacent row. In particular, bases 4 positioned within a row will overlap with two bases 4 in an adjacent row, whereas bases 4 positioned at the end of a row will usually overlap only one base 4 in an adjacent row.
As also shown in FIG. 2, the centers of the lands between adjacent rows are spaced apart a distance 16 in the range of about 0.157 cm to 0.291 cm, and preferably about 0.190 cm to 0.258 cm, with a preferred value being about 0.224 cm.
The calender roll according to the present invention can be constructed with various materials, such as steel including ANSI 1030 or better engravable steel. Moreover, the lands can be formed in any manner, such as by etching.
The above-described patterned calender roll is utilizable in the method of the present invention which includes thermally bonding fibers together to form a nonwoven fabric utilizing the calendar roll to form bond spots in the nonwoven fabric. For example, heat and pressure can be applied to the web in the nip between the calender roll of the present invention and a smooth roll for thermally bonding the fibers with a pattern of lands that form bonding points. By applying heat and pressure in the calender nip, portions of the fiber are fused or melted together to form the bond points. The pressure and temperature will vary with the material of the web to be bonded. The temperature can range over a wide range of temperatures, such as from about 110° C. to 220° C. Preferably, wherein the fibers comprise polypropylene, the rolls are heated to a temperature of about 135° C. to 200° C., more preferably about 140° C. to 185° C., and even more preferably about 140° C. to 180° C., and apply a pressure of about 160 to 480 pounds per linear inch, more preferably about 180 to 300 pounds per linear inch, with a preferred valued being about 240 pounds per linear inch. The bond points and non-bonded areas contribute to the strength of the nonwoven material, as well as its softness, stretchability, and elongation properties.
The fibers useful in accordance with the present invention can comprise various polymers. Thus, polymers useful with the present invention can comprise various spinnable polymeric materials such as polyolefins and blends comprising polyolefins. Preferably, the polymer is a polypropylene or a blend comprising a polypropylene. The polypropylene can comprise any polypropylene that is spinnable. The polypropylene can to be atactic, heterotactic, syndiotactic, isotactic and stereoblock polypropylene—including partially and fully isotactic, or at least substantially fully isotactic—polypropylenes. Polypropylenes which may be spun in the inventive system can be produced by any process. For example, the polypropylene can be prepared using Zeigler-Natta catalyst systems, or using homogeneous or heterogeneous metallocene catalyst systems.
Further, as used herein, the terms polymers, polyolefins, polypropylene, polyethylene, etc., include homopolymers, various polymers, such as copolymers and terpolymers, and mixtures (including blends and alloys produced by mixing separate batches or forming a blend in situ). When referring to polymers, the terminology copolymer is understood to include polymers of two monomers, or two or more monomers, including terpolymers. For example, the polymer can comprise copolymers of olefins, such as propylene, and these copolymers can contain various components. Preferably, in the case of polypropylene, such copolymers can include up to about 20 weight %, and, even more preferably, from about 0 to 10 weight % of at least one of ethylene and butene. However, varying amounts of these components can be contained in the copolymer depending upon the desired fiber.
Further, the polypropylene can comprise dry polymer pellet, flake or grain polymers having a narrow molecular weight distribution or a broad molecular weight distribution, with a broad molecular weight distribution being preferred. The term “broad molecular weight distribution” is here defined as dry polymer pellet, flake or grain preferably having an MWD value (i.e., Wt.Av.Mol.Wt./No.Av.Mol.Wt. measured by SEC as discussed below) of at least about 5, preferably at least about 5.5, more preferably at least about 6. Without limiting the invention, the MWD is typically about 2 to 15, more typically, less than about 10.
The resulting spun melt preferably has a weight average molecular weight varying from about 3×105 to about 5×105, a broad SEC molecular weight distribution generally in the range of about 6-20 or above, a spun melt flow rate, MFR, (determined according to ASTM D-1238-86 (condition L;230/2.16), which is incorporated by reference herein in its entirety) of about 13 to about 50 g/10 minutes, and/or a spin temperature conveniently within the range of about 220°-315° C., preferably about 300° C.
Still further, the polypropylene can be linear or branched, such as disclosed by U.S. Pat. No. 4,626,467 to Hostetter, which is incorporated by reference herein in its entirety, and is preferably linear. Additionally, in making the fiber of the present invention, the polypropylene to be made into fibers can include polypropylene compositions as taught in Gupta et al. U.S. Pat. No. 5,629,080, and European Patent Application No. 0 552 013 to Gupta et al., which are incorporated by reference herein in their entireties. Still further, polymer blends such as disclosed in Kozulla, U.S. Pat. application Ser. No. 08/358,884, filed Dec. 19, 1994, and Kozulla, U.S. Pat. application Ser. No. 08/998,592, filed Dec. 29, 1997, and European Patent Application No. 0 719 879, which are incorporated by reference in their entireties, can also be utilized. Yet further, polymer blends, especially polypropylene blends, which comprise a polymeric bond curve enhancing agent, as disclosed in U.S. patent application Ser. No. 08/728,491, to Harrington et al. and WO 97/37065, incorporated by reference as if set forth in their entirety herein, can also be utilized.
The production of polymer fibers for nonwoven materials usually involves the use of a mix of at least one polymer with nominal amounts of additives, such as antioxidants, stabilizers, pigments, antacids, process aids and the like. Thus, the polymer or polymer blend can include various additives, such as melt stabilizers, antioxidants, pigments, antacids and process aids. The types, identities and amounts of additives can be determined by those f ordinary skill in the art upon consideration of requirements of the product. Without limiting the invention, preferred antioxidants include Irganox 1076, and Irgafos 168 (both from Ciba-Geigy, Tarrytown, N.Y.) which may typically be present in the polymer composition in amounts of about 50-150 ppm (Irganox 1076) or about 200-1000 ppm (Irgafos 168) based on the weight of the total composition. Other optional additives which can be included in the fiber of the present invention include, for example, pigments such as titanium dioxide, typically in amounts up to about 2 weight %, antacids such as calcium stearate, typically in amounts ranging from about 0.01-0.2 weight %, colorants, typically in amounts ranging from 0.01-2.0 weight %, and other additives.
Various finishes can be applied to the filaments to maintain or render them hydrophilic or hydrophobic. Also, one or more components can be included in the polymer blend for modifying the surface properties of the fiber, such as to provide the fiber with repeat wettability, or to prevent or reduce build-up of static electricity. Hydrophobic finish compositions preferably include antistatic agents. Hydrophilic finishes may also include such agents.
Preferable hydrophobic finishes include those of U.S. Pat. No. 4,938,832, European Patent Application No. 486,158, all to Schmalz, which are incorporated by reference as if set forth in their entireties herein. These documents describe fiber finish compositions containing at least one neutralized phosphoric acid ester having a lower alkyl group, such as a 1-8 carbon alkyl group, which functions as an antistat, in combination with polysiloxane lubricants.
Another hydrophobic finish composition that can be used with the present invention is disclosed in U.S. Pat. No. 5,403,426, to Johnson et al., incorporated by reference as if set forth in its entirety herein. This patent describes a method of preparing hydrophobic fiber for processing inclusive of crimping, cutting, carding, compiling and bonding. The surface modifier comprises one or more of a class of water soluble compounds substantially free of lipophilic end groups and of low or limited surfactant properties.
Yet another hydrophobic finish composition that can be used with the present invention is disclosed in U.S. patent application Ser. No. 08/728,490, filed Oct. 9, 1996, to Hirwe et al. and WO 98/15685, which are incorporated by reference as if set forth in their entirety herein. The hydrophobic finish compositions of these documents comprise hydrophobic esters of pentaerythritol homologs, preferably hydrophobic esters of pentaerythritol and pentaerythritol oligomers. Finish compositions comprising such a lubricant may further comprise other lubricants, anti-static agents, and/or other additives.
Further, U.S. Pat. No. 5,540,953, to Harrington, incorporated by reference as if set forth in its entirety herein, describes antistatic compositions useful in the preparation of hydrophobic fibers and nonwoven fabrics. One finish described therein comprises 1) at least one neutralized C3-C12 alkyl or alkenyl phosphate alkali metal or alkali earth metal salt, and 2) a solubilizer. A second finish described therein comprises at least one neutralized phosphoric ester salt.
Other ingredients that may comprise a finish composition useful with the present invention include emulsifiers or other stabilizers, and preservatives such as biocides. One preferred biocide is Nuosept® 95, 95% hemiacetals in water, available from Nuodex Inc. division of HULS America Inc. (Piscataway, N.J.).
Finish compositions comprising hydrophilic finishes or other hydrophobic finishes, may be selected by those of ordinary skill in the art according to the characteristics of the apparatus and the needs of the product being manufactured. Other additives such as antistatic agents, stabilizers, emulsifiers and preservatives may be similarly selected.
The fibers are preferably polypropylene fibers, and more preferably are polypropylene fibers formed as skin-core fibers.
Fibers without a skin-core structure can be prepared by providing conditions which result in the manufacture of fibers without a skin-core structure. Such conditions may be achieved, for example, by providing an environment that sufficiently avoids oxidation of the surface of the filaments.
Fibers with a skin-core structure can be produced by any procedure that achieves oxidation, degradation and/or lowering of molecular weight of the polymer blend at the surface of the fiber as compared to the polymer blend in an inner core of the fiber. Such a skin-core structure can be obtained, for example, through a delayed quench and exposure to an oxidative environment, as disclosed in U.S. Pat. Nos. 5,431,994, 5,318,735 and 5,281,378, all to Kozulla, and European Application No. 719 879 A2, all of which are incorporated above by reference. Another method of obtaining a skin-core structure involves employing a heated spinnerette to achieve thermal degradation of the filament surface, as disclosed in U.S. Pat. No. 5,705,119 to Takeuchi et al., and European Patent Application No. 0 630 996, all of which are incorporated above by reference. As discussed in U.S. patent application Ser. No. 08/728,491 to Harrington et al. and WO 97/37065, incorporated by reference as if set forth in their entirety herein, the skin-core structure can comprise a skin showing an enrichment of ruthenium staining of at least about 0.2 μm, more preferably at least about 0.5 μm, more preferably at least about 0.7 μm, even more preferably at least about 1 μm, and even more preferably at least about 1.5 μm.
With fibers having a denier less than 2 dpf, another manner of stating the ruthenium enrichment is with respect to the equivalent diameter of the fiber, wherein the equivalent diameter is equal to the diameter of a circle with equivalent cross-section area of the fiber averaged over five samples. More particularly, for fibers having a denier less than 2, the skin thickness can also be stated in terms of enrichment in staining of the equivalent diameter of the fiber. In such an instance, the enrichment in ruthenium. staining can comprise at least about 1% and up to about 25% of the equivalent diameter of the fiber, preferably about 2% to 10% of the equivalent diameter of the fiber. Still further, the skin-core structure of the instant invention can be determined using a hot stage test, as disclosed in U.S. Pat. No. 5,705,119 to Takeuchi which is incorporated by reference herein, and a skin-core structure is present when a residue trail is present.
The skin-core structure comprises chemical modification of a filament to obtain the skin-core structure, and does not comprise separate components being joined along an axially extending interface, such as in sheath-core and side-by-side bicomponent fibers. Of course, the skin-core structure can be utilized in a composite fiber, such as the skin-core structure being present in the sheath of a sheath-core fiber in the manner disclosed in U.S. Pat. Nos. 5,281,378, 5,318,735 and 5,431,994 and EP Application No. 719 879 A2, which were discussed above and incorporated herein.
Thus, skin-core fibers can be prepared by providing conditions in any manner so that during extrusion of the polymer blend a skin-core structure is formed. For example, the temperature of a hot extrudate, such as an extrudate exiting a spinnerette, can be provided that is sufficiently elevated and for a sufficient amount of time within an oxidative atmosphere in order to obtain the skin-core structure. This elevated temperature can be achieved using a number of techniques, such as disclosed in the above discussed patents to Kozulla, and in U.S. and foreign applications to Takeuchi et al., discussed above and incorporated herein.
For example, skin-core filaments can be prepared in the inventive system through the method of U.S. Pat. Nos. 5,281,378, 5,318,735 and 5,431,994 to Kozulla, and European Patent Application No. 719 879 A2 in which the temperature of the hot extrudate can be provided above at least about 250° C. in an oxidative atmosphere for a period of time sufficient to obtain the oxidative chain scission degradation of its surface. This providing of the temperature can be obtained by delaying cooling of the hot extrudate as it exits the spinnerette, such as by blocking the flow of a quench gas reaching the hot extrudate. Such blocking can be achieved by the use of a shroud or a recessed spinnerette that is constructed and arranged to provide the maintaining of temperature.
In another aspect, as disclosed in U.S. Pat. No. 5,705,199 to Takeuchi et al., and European Patent Application No. 0 630 996, the skin-core structure can be obtained by heating the polymer blend in the vicinity of the spinnerette, either by directly heating the spinnerette or an area adjacent to the spinnerette. In other words, the polymer blend can be heated at a location at or adjacent to the at least one spinnerette, by directly heating the spinnerette or an element such as a heated plate positioned approximately 1 to 4 mm above the spinnerette, so as to heat the polymer composition to a sufficient temperature to obtain a skin-core fiber structure upon cooling, such as being immediately quenched, in an oxidative atmosphere.
In an application of the Takeuchi system to the present invention, for example, the extrusion temperature of the polymer may be about 230° C. to 250° C., and the spinnerette may have a temperature at its lower surface of preferably at least about 250° C. across the exit of the spinnerette in order to obtain oxidative chain scission degradation of the molten filaments to thereby obtain filaments having a skin-core structure. By the use of a heated spinnerette, therefore, the polymer blend is maintained at a sufficiently high temperature that upon extrusion from the spinnerette, oxidative chain scission occurs under oxidative quench conditions.
While the above techniques for forming the skin-core structure have been described, skin-core fibers prepared in the inventive system are not limited to those obtained by the above-described techniques. Any technique that provides a skin-core structure to the fiber is included in the scope of this invention.
In order to determine whether a skin-core fiber is present, a ruthenium staining test is utilized. As is disclosed in the above-noted U.S. and European applications to Takeuchi et al., which are incorporated by reference herein in their entirety, the substantially non-uniform morphological structure of the skin-core fibers according to the present invention can be characterized by transmission electron microscopy (TEM) of ruthenium tetroxide (RuO4)-stained fiber thin sections. In this regard, as taught by Trent et al., in Macromolecules, Vol. 16, No. 4, 1983, “Ruthenium Tetroxide Staining of Polymers for Electron Microscopy”, which is hereby incorporated by reference in its entirety, it is well known that the structure of polymeric materials is dependent on their heat treatment, composition, and processing, and that, in turn, mechanical properties of these materials such as toughness, impact strength, resilience, fatigue, and fracture strength can be highly sensitive to morphology. Further, this article teaches that transmission electron microscopy is an established technique for the characterization of the structure of heterogeneous polymer systems at a high level of resolution; however, it is often necessary to enhance image contrast for polymers by use of a staining agent. Useful staining agents for polymers are taught to include osmium tetroxide and ruthenium tetroxide. For the staining of the fibers of the present invention, ruthenium tetroxide is the preferred staining agent.
In the morphological characterization of the present invention, samples of fibers are stained with aqueous RuO4, such as a 0.5% (by weight) aqueous solution of ruthenium tetroxide obtainable from Polysciences, Inc., overnight at room temperature. (While a liquid stain is utilized in this procedure, staining of the samples with a gaseous stain is also possible.) Stained fibers are embedded in Spurr epoxy resin and cured overnight at 60° C. The embedded stained fibers are then thin sectioned on an ultramicrotome using a diamond knife at room temperature to obtain microtomed sections approximately 80 nm thick, which can be examined on conventional apparatus, such as a Zeiss EM-10 TEM, at 100 kV. Energy dispersive x-ray analysis (EDX) was utilized to confirm that the RuO4 had penetrated completely to the center of the fiber.
According to the present invention, the ruthenium staining test would be performed to determine whether a skin-core structure is present in a fiber. More specifically, a fiber can be subjected to ruthenium staining, and the enrichment of ruthenium (Ru residue) at the outer surface region of the fiber cross-section would be determnined. If the fiber shows an enrichment in the ruthenium staining for a thickness of at least about 0.2 μm or at least about 1% of the equivalent diameter for fibers having a denier of less than 2, the fiber has a skin-core structure.
While the ruthenium staining test is an excellent test for determining skin-core structure, there may be certain instances wherein enrichment in ruthenium staining may not occur. For example, there may be certain components within the fiber that would interfere with or prevent the ruthenium from showing an enrichment at the skin of the fiber, when, in fact, the fiber comprises a skin-core structure. The description of the ruthenium staining test herein is in the absence of any materials and/or components that would prevent, interfere with, or reduce the staining, whether these materials are in the fiber as a normal component of the fiber, such as being included therein as a component of the processed fiber, or whether these materials are in the fiber to prevent, interfere with or reduce ruthenium staining.
As discussed above, the present invention utilizes nonwoven materials including the fibers described above which are thermally bonded together. In particular, by incorporating the skin-core fibers described above into nonwoven materials, the resulting nonwoven materials possess exceptional cross-directional strength, softness and elongation properties. These nonwoven materials can be used as at least one layer in various products, including hygienic products, such as sanitary napkins, incontinence products and diapers, comprising at least one liquid absorbent layer and at least one nonwoven material layer of the present invention and/or incorporating fibers of the present invention thermally bonded together. Further, as previously indicated, the articles according to the present invention can include at least one liquid permeable or impermeable layer. For example, a diaper incorporating a nonwoven fabric of the present invention would include, as one embodiment, an outermost impermeable or permeable layer, an inner layer of the nonwoven material, and at least one intermediate absorbent layer. Of course, a plurality of nonwoven material layers and absorbent layers can be incorporated in the diaper (or other hygienic product) in various orientations, and a plurality of outer permeable and/or impermeable layers can be included for strength considerations.
Further, the nonwovens of the present invention can include a plurality of layers, with the layers being of the same fibers or different. Further, not all of the layers need include skin-core fibers of the polymer blend described above. For example, the nonwovens of the present invention can be used by themselves or in combination with other nonwovens, or in combination with other nonwovens or films.
Examples of suitable fibers are the following which are skin-core polypropylene fibers available from Hercules Incorporated, a Delaware corporation: T190 fiber which is a 2.2 dpf (denier-per-filament) staple fiber; T194 fiber which is a 2.6 dpf staple fiber; and T198 fiber which is a 2.6 dpf staple fiber.
The web may be a carded fibrous web or formed from continuous filaments and microfiber network structures, or from any of the many known conventional methods. The fibers can be formed in accordance with the process disclosed in co-pending U.S. application Ser. No. 08/728,491, filed Oct. 9, 1996, and WO 97/37065, the entire disclosures of which are expressly incorporated herein by reference.
Further, the fibers of the present invention can have any cross-sectional configuration, such as oval, circular, diamond, delta, trilobal—“Y”-shaped, “X”-shaped, and concave delta, wherein the sides of the delta are slightly concave. Preferably, the fibers include a circular or a concave delta cross-section configuration. The cross-sectional shapes are not limited to these examples, and can include other cross-sectional shapes. Additionally, the fibers can include hollow portions, such as a hollow fiber, which can be produced, for example, with a “C” cross-section spinnerette.
EXAMPLES
The invention generally described above is now further described with the following Examples. These Examples are meant to be illustrative of some embodiments of the invention, but are not meant to limit the invention in any way. Other embodiments, both as apparent to those in the art and as described above, are included in this invention, which is limited only by the claims. Unless otherwise noted, parts and percentages, etc., are by weight.
In the examples, normalized cross-directional strength and elongation were determined using test strips (six per sample) of each nonwoven, 1 inch×7 inches (25 mm×178 mm) using a tensile tester Model 1122 from Instron Corporation, Canton, Mass. Specifically, the breaking load and elongation are determined in accordance with the “cut strip test” in ASTM D-1682-64 (Re-approved 1975), which is incorporated by reference in its entirety, using the Instron Tester set at constant rate of traverse testing mode. The gauge length is 12.7 cm, the crosshead speed is 12.7 cm/minute, and the extension rate is 100%/minute.
Nonwoven fabrics were prepared by carding the fibers into conventional fiber webs at 250 feet per minute (76 m/min) using equipment and procedures as discussed in Legare, R. J., 1986 TAPPI Synthetic Fibers for Wet System and Thermal Bonding Applications, Boston Park Plaza Hotel & Towers, Boston, Mass. Oct. 9-10, 1986, “Thermal Bonding of Polypropylene Fibers in Nonwovens”, pages 1-13, 57-71 and attached Tables and Figures. The Webmaster® randomizers described in the TAPPI article were not used. This article is incorporated herein in its entirety, by reference thereto.
Two layers of the carded staple fibers were stacked in the machine direction, and bonded using either a calender roll according to the present invention (identified as Roll B in Tables I-III), and a known diamond design embossed calender roll (identified as Roll A in Tables I-III) and a smooth roll at roll temperatures ranging from about 145 to 170° C. and roll pressures of 420 Newtons per linear centimeter (240 pounds per linear inch) to obtain nonwovens weighing nominally about 23.9 grams per square meter (20±1 grams per square yard).
The diamond pattern calender roll had a 15% land area, 58.8 spots/sq.cm. with a depth of 0.076 cm. Further, the diamonds had a width (w) of 0.101 cm, a height (h) of 0.051 cm, and are spaced height-wise (H) 0.22 cm on center, and width-wise (L) 0.152 cm on center, as illustrated in FIG. 12.
The calender roll configured in accordance with the present invention (Roll B) was formed of ANSI 1030 engravable steel which was engraved to provide a plurality of lands, and ground in a cylindrical grinder to provide a minimum loss of outer diameter of the roll while keeping the roll concentric. Next the roll was polished to deburr and finished to 4-6 RMS. The resulting roll had a nominal diameter of approximately 24.65 cm and a length of about 57.15 cm, and the outer cylindrical surface included a plurality of lands having a truncated pyramidal shape, with a land or bond area of approximately 11% and 22 spots/sq.cm. Further, each truncated pyramidal shaped land had a rectangular base having a short side width (aligned in the machine or radial direction of the roll) of 0.107 cm, a long side length (aligned in the cross or longitudinal direction of the roll) of 0.158 cm, and a height of 0.76 cm. The upper surface of each land had short sides of 0.51 cm that extend parallel to the width of the base and had long sides of 0.102 cm that extend parallel to the length of the base. The sides of the lands tapered from the base to the upper surface at an angle of 20°.
The lands were provided on the outer peripheral surface and arranged in rows parallel to the longitudinal axis of the roll, and included 178 rows of 263 lands (short rows) alternating with 179 rows of 274 lands (long rows), respectively. The centers of the endmost lands in the short rows were spaced 2.007 cm from the roll ends, while the centers of the endmost lands in the long rows were spaced 0.244 cm from the roll ends. The centers of the lands of adjacent rows were spaced apart a distance of 0.224 cm (in the radial direction) and the distance from the center of a land in one row to the center of a land in an adjacent row (in the longitudinal direction of the roll) was 0.102 cm. Also, the distance between the bases in adjacent rows (in the radial direction) was 0.117 cm while the distance between bases in adjacent rows (in the longitudinal direction) was 0.046 cm.
The increased stretch or elongation of the thermal bonded skin-core polypropylene fabric formed in accordance with the present invention is demonstrated in Tables I-III and corresponding FIGS. 5-10 . Tables I-III compare the cross-directional strength (CDS) and cross-directional elongation (CDE) of fabrics formed of three different fibers, with each table comparing a fabric formed with a conventional patterned roll (Roll A) and with a patterned roll according to the present invention (Roll B). As shown in Table 1 for a T190 fiber with 2.2 DPF, and as depicted in FIGS. 5 and 6, the cross-directional strength for a fabric formed from a calender roll according to the present invention (curve 17) is somewhat less than that formed by the conventional calender roll (curve 18). However, and importantly, the cross-directional elongation of the fabric formed in accordance with the present invention (curve 19) has greatly increased elongation as compared to that formed by the conventional calender roll (curve 20).
TABLE I
T190 2.2 DPF FIBER
BOND
TEMP Roll A Roll B Roll A Roll B
° C. CDS CDS CDE CDE
148 178 123
151 204 135
154 285 184 71 159
157 343 298 76 169
160 375 294 86 150
163 454 314 96 162
166 472 302 91 143
169 452 319 87 154
172 412 242 76 114
Turning to the Table II data which is for a T198 fiber with 2.6 DPF, and the Table III data which is for a T194 fiber with a 2.6 DPF, similar results can be seen when comparing the fabric formed with these fibers by the conventional calender roll A (curves 21, 23, 25 and 27 as depicted in FIGS. 7-10) when compared with the patterned roll B according to the present invention (curves 22, 24, 26, 28 as depicted in FIGS. 7-10).
TABLE II
T198 2.6 DPF FIBER
BOND
TEMP Roll A Roll B Roll A Roll B
° C. CDS CDS CDE CDE
148 154 107
151 431 226 79 131
154 480 255 87 146
157 594 267 100 147
160 672 261 106 140
163 609 223 82 119
166 679 236 87 124
169 463 191 57 97
172 502 214 62 108
175 382 49
TABLE III
T194 2.6 DPF FIBER
BOND
TEMP Roll A Roll B Roll A Roll B
° C. CDS CDS CDE CDE
148 200 180
151 226 199
154 231 190
157 439 250 125 199
160 506 259 142 200
163 439 252 111 178
166 525 210 121 154
169 400 216 89 151
172 371 78
175 382 76
Accordingly, it can be seen that by using the calender roll having the pattern of lands according to the present invention in the method according to the present invention and utilizing skin-core polypropylene fibers result in a thermal bonded fabric having a much greater stretchability or elongation than that of thermal bonded fabrics formed with a roller having a conventional pattern.
Although the invention has been described herein with reference to particular means, materials and embodiments, the invention is not intended to be limited to the particulars disclosed herein; rather, the invention extends to all fuinctionally equivalent structures, methods and uses, such as are within the scope of the appended claims.

Claims (26)

What is claimed is:
1. A method of manufacturing thermally bonded fabric, the method comprising:
forming a web of thermally bondable polypropylene fibers;
passing said web over a heated calender roll having a patterned surface including a plurality of rows of lands, with each of said lands having an upper surface, with upper surfaces of lands in adjacent rows of lands being staggered such that they do not overlap one another in a machine direction; and
thermally bonding the fibers at bond points located about the upper surfaces of the lands such that fibers extending in the machine direction or substantially in the machine direction will only have one bond point for adjacent rows of lands.
2. The method according to claim 1, wherein said polypropylene fibers are skin core polypropylene fibers.
3. The method according to claim 2, further comprising providing the web as a carded fibrous web.
4. The method according to claim 2, further comprising providing the web as a plurality of continuous filaments.
5. The method according to claim 2, wherein said elongation is at least about 120%.
6. The method according to claim 5, wherein said elongation is greater than about. 140%.
7. The method according to claim 6, wherein said elongation is greater than about 160%.
8. The method according to claim 7, wherein said elongation is greater than about 180%.
9. The method according to claim 8, wherein said elongation is greater than about 200%.
10. The method according to claim 9, wherein said elongation is greater than about 250%.
11. The method according to claim 10, wherein said elongation is greater than about 300%.
12. The method according to claim 2, wherein the passing said web over a heated calender roll comprises:
passing said fibrous web between a pair of cooperating rolls in a calender nip, at least one of said pair of rolls having said patterned surface and comprising a cylindrical roll having an outer cylindrical surface including a plurality of lands;
said lands being arranged on said outer cylindrical surface in a plurality of spaced apart rows;
each of said lands comprising a tapered shape including a base tapering to an upper surface;
said upper surface including short sides of about 0.036 cm to 0.066 cm in length oriented in a machine direction and long sides of about 0.071 cm to 0.133 cm in length oriented in a cross direction;
adjacent rows of said lands being spaced apart a distance, with respect to the centers of said lands, of about 0.157 cm to 0.291 cm;
upper surfaces of lands in adjacent rows being staggered such that upper surfaces in adjacent rows do not overlap with one another in a machine direction providing a plurality of spaced apart bond points capable of bonding fibers extending in the machine direction or substantially in the machine direction at only one bond point for adjacent rows; and
said plurality of lands providing a bond area up to about 20%.
13. The method according to claim 12, wherein said upper surfaces are substantially rectangular.
14. The method according to claim 13, wherein said bases overlap in the machine direction in adjacent rows.
15. The method according to claim 14, wherein said bond area ranges from about 5% to 20%.
16. The method according to claims 15, wherein said bond area is in the range of about 8% to about 12%.
17. The method according to claim 16, wherein said bond area is about 11%.
18. The method according to claim 15, wherein said bond area is in the range of about 8% to about 15%.
19. The method according to claim 18, wherein centers of said lands in each row are spaced apart by a distance of about 0.142 cm to 0.264 cm, and centers of said lands in adjacent rows are spaced apart by a distance of about 0.071 cm to 0.133 cm.
20. The method according to claim 18, wherein said lands are constructed and arranged such that a straight fiber lying at an angle of about 35° to 55° with respect to the machine direction is positioned in a space between said lands, whereby the fiber is not bonded.
21. The method according to claim 20, wherein said lands are constructed and arranged such that a straight fiber lying at an angle of about 45° with respect to the machine direction is positioned in a space between said lands, whereby the fiber is not bonded.
22. The method according to claim 18, wherein said lands are of a truncated pyramidal shape, each having a substantially rectangular base with short sides about 0.075 cm to 0.139 cm in length oriented in the machine direction and long sides about 0.111 cm to 0.205 cm in length oriented in the cross direction, and tapered side walls extending between the base and the upper surface at an angle α of about 14° to 35°.
23. The method according to claim 22, wherein said tapered side walls extend between the base and the upper surface at an angle a of about 17° to 23°.
24. The method according to claim 18, wherein:
said lands are of a truncated pyramidal shape having an upper surface with short sides of about 0.043 cm to 0.059 cm in length oriented in a machine direction and long sides of about 0.087 cm to 0.117 cm in length oriented in a cross direction;
adjacent rows of said lands being spaced apart a distance, with respect to the centers of said lands, of about 0.190 cm to 0.258 cm;
centers of said lands in each row are spaced apart by a distance of about 0.173 cm to 0.233 cm, and centers of said lands in adjacent rows are spaced apart by a distance of about 0.087 cm to 0.117 cm;
said lands are constructed and arranged such that a straight fiber lying at an angle of about 45° with respect to the machine direction is positioned in a space between said lands, whereby the fiber is not bonded; and
said truncated pyramidal shape lands each have a substantially rectangular base with short sides about 0.091 cm to 0.123 cm in length oriented in the machine direction and long sides about 0.134 to 0.182 cm in length oriented in the cross directi6n, and tapered side walls extending between the base and the upper surface at an angle a of about 17° to 26°.
25. The method according to claim 18, wherein:
each of said lands comprising a truncated pyramidal shape having an upper surface with short sides of about 0.051 cm in length oriented in a machine direction and long sides of about 0.102 cm in length oriented in a cross direction;
adjacent rows of said lands being spaced apart a distance, with respect to the centers of said lands, of about 0.224 cm;
centers of said lands in each row are spaced apart by a distance of about 0.203 cm, and centers of said lands in adjacent rows are spaced apart by a distance of about 0.102 cm;
said lands are constructed and arranged such that a straight fiber tying at an angle of about 45° with respect to the machine direction is positioned in a space between said lands, whereby the fiber is not bonded; and
said truncated pyramidal shape lands each have a substantially rectangular base with short sides about 0.107 cm in length oriented in the machine direction and long sides about 0.158 cm in length oriented in the cross direction, and tapered side walls extending between the base and the upper surface at an angle α of about 17° to 23°.
26. A method of manufacturing thermally bonded fabric, the method comprising:
forming a web comprising thermally bondable skin-core polypropylene fibers;
passing said web over a calender roll having a patterned surface including a plurality of rows of lands, with each of said lands having an upper surface, with upper surfaces of lands in adjacent rows of lands being staggered such that they do not overlap one another in a machine direction;
applying heat and pressure to said fibrous web at a location of said calender roll to thermally bond the fibers at bond points located about the upper surfaces of the lands such that fibers extending in the machine direction or substantially in the machine direction will only have one bond point for adjacent rows of lands.
US09/116,371 1998-07-16 1998-07-16 Method and apparatus for thermal bonding high elongation nonwoven fabric Expired - Lifetime US6752947B1 (en)

Priority Applications (7)

Application Number Priority Date Filing Date Title
US09/116,371 US6752947B1 (en) 1998-07-16 1998-07-16 Method and apparatus for thermal bonding high elongation nonwoven fabric
EP99933486A EP1144741A3 (en) 1998-07-16 1999-07-08 Method and apparatus for thermal bonding high elongation nonwoven fabric
CA002336834A CA2336834A1 (en) 1998-07-16 1999-07-08 Method and apparatus for thermal bonding high elongation nonwoven fabric
AU49533/99A AU4953399A (en) 1998-07-16 1999-07-08 Method and apparatus for thermal bonding high elongation nonwoven fabric
CN99810479A CN1321119A (en) 1998-07-16 1999-07-08 Method and apparatus for thermal bonding high elongation nonwoven fabric
JP2000560304A JP2002522648A (en) 1998-07-16 1999-07-08 Method and apparatus for thermally bonded high elongation nonwoven fabric
PCT/US1999/012370 WO2000004215A2 (en) 1998-07-16 1999-07-08 Method and apparatus for thermal bonding high elongation nonwoven fabric

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US09/116,371 US6752947B1 (en) 1998-07-16 1998-07-16 Method and apparatus for thermal bonding high elongation nonwoven fabric

Publications (1)

Publication Number Publication Date
US6752947B1 true US6752947B1 (en) 2004-06-22

Family

ID=22366771

Family Applications (1)

Application Number Title Priority Date Filing Date
US09/116,371 Expired - Lifetime US6752947B1 (en) 1998-07-16 1998-07-16 Method and apparatus for thermal bonding high elongation nonwoven fabric

Country Status (7)

Country Link
US (1) US6752947B1 (en)
EP (1) EP1144741A3 (en)
JP (1) JP2002522648A (en)
CN (1) CN1321119A (en)
AU (1) AU4953399A (en)
CA (1) CA2336834A1 (en)
WO (1) WO2000004215A2 (en)

Cited By (14)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US20060128247A1 (en) * 2004-12-14 2006-06-15 Kimberly-Clark Worldwide, Inc. Embossed nonwoven fabric
US20070048498A1 (en) * 2005-08-29 2007-03-01 Cree James W Apertured Laminate and Method of Making
US20070249253A1 (en) * 2006-04-24 2007-10-25 Piero Angeli Elastic laminate comprising elastic substrate between extensible webs and method for making
US20090191779A1 (en) * 2008-01-30 2009-07-30 Cree James W Elastic laminate and method of making
US20100305543A1 (en) * 2007-08-16 2010-12-02 Frantisek Klaska Nonwoven fabric and method for the production thereof
US20110151185A1 (en) * 2009-12-18 2011-06-23 Cree James W Extrusion coated perforated nonwoven web and method for making
USD702047S1 (en) 2012-10-15 2014-04-08 Polymer Group, Inc. Nonwoven fabric
USD714560S1 (en) 2012-09-17 2014-10-07 The Procter & Gamble Company Sheet material for an absorbent article
US9067334B2 (en) 2009-03-24 2015-06-30 Advantage Creation Enterprise Llc Embossed textured webs and method for making
US9096961B2 (en) 2012-04-27 2015-08-04 Providencia Usa, Inc. Nonwoven wipe with bonding pattern
US9408761B2 (en) 2011-03-25 2016-08-09 The Procter & Gamble Company Article with nonwoven web component formed with loft-enhancing calendar bond shapes and patterns
US20180002851A1 (en) * 2016-03-10 2018-01-04 Reifenhaeuser Gmbh & Co. Kg Maschinenfabrik Weldable spunbond fabric, method of making same, and packaging made therefrom
US10828209B2 (en) 2015-12-16 2020-11-10 Avintiv Specialty Materials Inc. Soft nonwoven fabric and method of manufacturing thereof
USD907931S1 (en) * 2018-05-22 2021-01-19 Berry Global, Inc. Nonwoven fabric

Families Citing this family (10)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US6610390B1 (en) * 1999-08-13 2003-08-26 First Quality Nonwovens, Inc. Nonwoven with non-symmetrical bonding configuration
US6901609B2 (en) 2001-01-15 2005-06-07 The Procter & Gamble Company Method of dispensing volatile and soluble substances and a device for use therein
DE102005015550C5 (en) * 2005-04-04 2013-02-07 Carl Freudenberg Kg Use of a thermally bonded nonwoven fabric
DE102005025055B4 (en) * 2005-05-30 2007-12-06 Fiberweb Corovin Gmbh A process for producing a high extensibility nonwoven fabric from polymer blends comprising amphiphilic block copolymers, high extensibility nonwoven web and use, and polymer blends for producing a high extensibility nonwoven web
CZ2012655A3 (en) 2012-09-21 2014-04-02 Pegas Nonwovens S.R.O. Nonwoven fabric with enhanced softness and process for preparing such fabric
KR101349894B1 (en) 2013-09-27 2014-01-13 박태연 Embossed oriented nonwoven composites and manufacturing apparatus the same
DE102015120318B4 (en) * 2015-11-24 2021-05-06 Webasto SE Method for producing a roller blind for a roller blind arrangement of a vehicle and roller blind arrangement
WO2017095583A1 (en) 2015-11-30 2017-06-08 The Procter & Gamble Company Nonwoven thermal bonding pattern with low fuzz
EP3383333B1 (en) 2015-11-30 2020-10-21 The Procter and Gamble Company Nonwoven thermal bonding pattern with low fuzz
CN105887337A (en) * 2016-06-03 2016-08-24 佛山市格菲林卫材科技有限公司 Production system and method for ultra-soft hydrophobic non-woven fabric

Citations (54)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US1945024A (en) 1930-04-21 1934-01-30 Mapes Cons Mfg Co Packing material for fragile articles
US1958050A (en) 1930-02-18 1934-05-08 Holed Tite Packing Corp Packing material
US2352194A (en) 1937-09-13 1944-06-27 Josef A Grabec Method of molding perforated elastic material
US2464301A (en) 1943-12-18 1949-03-15 American Viscose Corp Textile fibrous product
US3081514A (en) 1954-06-16 1963-03-19 Johnson & Johnson Foraminous nonwoven fabric
US3323983A (en) 1964-09-08 1967-06-06 Kimberly Clark Co Apparatus for embossing multi-ply paper sheets
US3616157A (en) * 1969-08-08 1971-10-26 Johnson & Johnson Embossed nonwoven wiping and cleaning materials
US3855046A (en) 1970-02-27 1974-12-17 Kimberly Clark Co Pattern bonded continuous filament web
US3868287A (en) 1971-04-27 1975-02-25 Scott Paper Co Absorbent pad and method for making same
US3949128A (en) 1972-08-22 1976-04-06 Kimberly-Clark Corporation Product and process for producing a stretchable nonwoven material from a spot bonded continuous filament web
US4110152A (en) 1975-06-20 1978-08-29 Avery International Corporation Embossing roller and method
FR2411260A1 (en) 1977-05-24 1979-07-06 Monsanto Co Isotropic fibre fleece mfr. - from anisotropic fleece with random oriented fibres, by passing through nip of embossed rollers to produce pattern of joins
US4248822A (en) 1978-02-15 1981-02-03 Lever Brothers Company Process and apparatus for producing a moisture-permeable film
US4278482A (en) 1979-06-26 1981-07-14 Custom Coating, Inc. Apparatus and method for production of polyurethane carpet backing
US4333979A (en) 1980-08-18 1982-06-08 Kimberly-Clark Corporation Soft, bulky, lightweight nonwoven web and method of producing; the web has both fused spot bonds and patterned embossments
US4374888A (en) 1981-09-25 1983-02-22 Kimberly-Clark Corporation Nonwoven laminate for recreation fabric
US4419160A (en) 1982-01-15 1983-12-06 Burlington Industries, Inc. Ultrasonic dyeing of thermoplastic non-woven fabric
US4422837A (en) 1974-12-10 1983-12-27 Rasmussen O B Apparatus for converting thermoplastic film into an open-work sheet
US4443512A (en) 1981-09-22 1984-04-17 Colgate-Palmolive Company Absorbent article with densified areas
US4473432A (en) 1983-02-04 1984-09-25 Harold Leader Dot heat stapling
US4483728A (en) 1980-07-14 1984-11-20 Kimberly-Clark Corporation Relieved patterned marrying roll
US4493868A (en) 1982-12-14 1985-01-15 Kimberly-Clark Corporation High bulk bonding pattern and method
US4614632A (en) 1983-12-30 1986-09-30 Nippon Petrochemicals Company, Limited Method and apparatus for continuously forming embossed sheets
US4626467A (en) 1985-12-16 1986-12-02 Hercules Incorporated Branched polyolefin as a quench control agent for spin melt compositions
US4741944A (en) 1986-07-30 1988-05-03 Kimberly-Clark Corporation Wet wipe and wipe dispensing arrangement
US4817788A (en) 1984-11-28 1989-04-04 The Procter & Gamble Company Laminated laundry product
US4902366A (en) 1987-01-10 1990-02-20 Corovin Gmbh Process and apparatus for bonding and embossing sheet materials, particularly fiber matting
US4938832A (en) 1989-05-30 1990-07-03 Hercules Incorporated Cardable hydrophobic polypropylene fiber, material and method for preparation thereof
USD311997S (en) 1987-06-26 1990-11-13 Hercules Incorporated Embossed diaper cover stock material or similar article
USD313319S (en) 1987-06-26 1991-01-01 Hercules Incorporated Embossed diaper cover stock or similar article
USD314672S (en) 1987-06-26 1991-02-19 Hercules Incorporated Embossed diaper cover stock or similar article
USD314673S (en) 1987-07-13 1991-02-19 Hercules Incorporated Embossed diaper cover stock material or similar article
US5036758A (en) 1987-09-21 1991-08-06 Mitsui Petrochemical Industries, Ltd. Emboss roll
US5057357A (en) 1988-10-21 1991-10-15 Fiberweb North America, Inc. Soft coverstock with improved dimensional stability and strength and method of manufacturing the same
EP0486158A2 (en) 1990-11-15 1992-05-20 Hercules Incorporated Cardable hydrophobic polyolefin fiber, material and method for preparation thereof
US5128193A (en) 1990-01-16 1992-07-07 Chicopee Absorbent fibrous structure
US5156863A (en) 1982-09-30 1992-10-20 Stimsonite Corporation Continuous embossing belt
US5158819A (en) 1990-06-29 1992-10-27 The Procter & Gamble Company Polymeric web exhibiting a soft, silky, cloth-like tactile impression and including a contrasting visually discernible pattern having an embossed appearance on at least one surface thereof
EP0552013A2 (en) 1992-01-13 1993-07-21 Hercules Incorporated Thermally bondable fiber for high strength non-woven fabrics
US5281378A (en) 1990-02-05 1994-01-25 Hercules Incorporated Process of making high thermal bonding fiber
US5296289A (en) 1992-04-29 1994-03-22 Collins Loren M Stretchable spun bonded nonwoven web and method
EP0630996A2 (en) 1993-06-24 1994-12-28 Hercules Incorporated Skin-core high thermal bond strength fiber on melt spin system
US5383778A (en) 1990-09-04 1995-01-24 James River Corporation Of Virginia Strength control embossing apparatus
US5403426A (en) 1991-05-28 1995-04-04 Hercules Incorporated Process of making cardable hydrophobic polypropylene fiber
EP0719879A2 (en) 1994-12-19 1996-07-03 Hercules Incorporated Process for producing fibers for high strength non-woven materials, and the resulting fibers and non-wovens
US5534208A (en) 1993-09-15 1996-07-09 Foamex L.P. Three dimensional surface shaping of synthetic foam pads by continuous rotary process
US5540953A (en) 1992-02-14 1996-07-30 Hercules Incorporated Process of preparing fabric comprising hydrophobic polyolefin fibers
US5580423A (en) 1993-12-20 1996-12-03 The Procter & Gamble Company Wet pressed paper web and method of making the same
US5620776A (en) 1992-12-24 1997-04-15 James River Corporation Of Virginia Embossed tissue product with a plurality of emboss elements
US5622734A (en) 1994-03-14 1997-04-22 Kimberly-Clark Corporation Apparatus for producing a crimp-bonded fibrous cellulosic laminate
US5656132A (en) 1993-06-24 1997-08-12 Kimberly-Clark Worldwide, Inc. Soft tissue
WO1997037065A1 (en) 1996-03-29 1997-10-09 Hercules Incorporated Polypropylene fibers and items made therefrom
WO1998015685A1 (en) 1996-10-09 1998-04-16 Hercules Incorporated Ester lubricants as hydrophobic fiber finishes
US5985193A (en) 1996-03-29 1999-11-16 Fiberco., Inc. Process of making polypropylene fibers

Patent Citations (59)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US1958050A (en) 1930-02-18 1934-05-08 Holed Tite Packing Corp Packing material
US1945024A (en) 1930-04-21 1934-01-30 Mapes Cons Mfg Co Packing material for fragile articles
US2352194A (en) 1937-09-13 1944-06-27 Josef A Grabec Method of molding perforated elastic material
US2464301A (en) 1943-12-18 1949-03-15 American Viscose Corp Textile fibrous product
US3081514A (en) 1954-06-16 1963-03-19 Johnson & Johnson Foraminous nonwoven fabric
US3323983A (en) 1964-09-08 1967-06-06 Kimberly Clark Co Apparatus for embossing multi-ply paper sheets
US3616157A (en) * 1969-08-08 1971-10-26 Johnson & Johnson Embossed nonwoven wiping and cleaning materials
US3855046A (en) 1970-02-27 1974-12-17 Kimberly Clark Co Pattern bonded continuous filament web
US3868287A (en) 1971-04-27 1975-02-25 Scott Paper Co Absorbent pad and method for making same
US3949128A (en) 1972-08-22 1976-04-06 Kimberly-Clark Corporation Product and process for producing a stretchable nonwoven material from a spot bonded continuous filament web
US4422837A (en) 1974-12-10 1983-12-27 Rasmussen O B Apparatus for converting thermoplastic film into an open-work sheet
US4110152A (en) 1975-06-20 1978-08-29 Avery International Corporation Embossing roller and method
FR2411260A1 (en) 1977-05-24 1979-07-06 Monsanto Co Isotropic fibre fleece mfr. - from anisotropic fleece with random oriented fibres, by passing through nip of embossed rollers to produce pattern of joins
US4248822A (en) 1978-02-15 1981-02-03 Lever Brothers Company Process and apparatus for producing a moisture-permeable film
US4278482A (en) 1979-06-26 1981-07-14 Custom Coating, Inc. Apparatus and method for production of polyurethane carpet backing
US4483728A (en) 1980-07-14 1984-11-20 Kimberly-Clark Corporation Relieved patterned marrying roll
US4333979A (en) 1980-08-18 1982-06-08 Kimberly-Clark Corporation Soft, bulky, lightweight nonwoven web and method of producing; the web has both fused spot bonds and patterned embossments
US4443512A (en) 1981-09-22 1984-04-17 Colgate-Palmolive Company Absorbent article with densified areas
US4374888A (en) 1981-09-25 1983-02-22 Kimberly-Clark Corporation Nonwoven laminate for recreation fabric
US4419160A (en) 1982-01-15 1983-12-06 Burlington Industries, Inc. Ultrasonic dyeing of thermoplastic non-woven fabric
US5156863A (en) 1982-09-30 1992-10-20 Stimsonite Corporation Continuous embossing belt
US4493868A (en) 1982-12-14 1985-01-15 Kimberly-Clark Corporation High bulk bonding pattern and method
US4473432A (en) 1983-02-04 1984-09-25 Harold Leader Dot heat stapling
US4614632A (en) 1983-12-30 1986-09-30 Nippon Petrochemicals Company, Limited Method and apparatus for continuously forming embossed sheets
US4817788A (en) 1984-11-28 1989-04-04 The Procter & Gamble Company Laminated laundry product
US4626467A (en) 1985-12-16 1986-12-02 Hercules Incorporated Branched polyolefin as a quench control agent for spin melt compositions
US4741944A (en) 1986-07-30 1988-05-03 Kimberly-Clark Corporation Wet wipe and wipe dispensing arrangement
US4902366A (en) 1987-01-10 1990-02-20 Corovin Gmbh Process and apparatus for bonding and embossing sheet materials, particularly fiber matting
USD313319S (en) 1987-06-26 1991-01-01 Hercules Incorporated Embossed diaper cover stock or similar article
USD314672S (en) 1987-06-26 1991-02-19 Hercules Incorporated Embossed diaper cover stock or similar article
USD311997S (en) 1987-06-26 1990-11-13 Hercules Incorporated Embossed diaper cover stock material or similar article
USD314673S (en) 1987-07-13 1991-02-19 Hercules Incorporated Embossed diaper cover stock material or similar article
US5036758A (en) 1987-09-21 1991-08-06 Mitsui Petrochemical Industries, Ltd. Emboss roll
US5057357A (en) 1988-10-21 1991-10-15 Fiberweb North America, Inc. Soft coverstock with improved dimensional stability and strength and method of manufacturing the same
US4938832A (en) 1989-05-30 1990-07-03 Hercules Incorporated Cardable hydrophobic polypropylene fiber, material and method for preparation thereof
US5128193A (en) 1990-01-16 1992-07-07 Chicopee Absorbent fibrous structure
US5318735A (en) 1990-02-05 1994-06-07 Hercules Incorporated Process of making high thermal bonding strength fiber
US5431994A (en) 1990-02-05 1995-07-11 Hercules Incorporated High thermal strength bonding fiber
US5281378A (en) 1990-02-05 1994-01-25 Hercules Incorporated Process of making high thermal bonding fiber
US5158819A (en) 1990-06-29 1992-10-27 The Procter & Gamble Company Polymeric web exhibiting a soft, silky, cloth-like tactile impression and including a contrasting visually discernible pattern having an embossed appearance on at least one surface thereof
US5383778A (en) 1990-09-04 1995-01-24 James River Corporation Of Virginia Strength control embossing apparatus
EP0486158A2 (en) 1990-11-15 1992-05-20 Hercules Incorporated Cardable hydrophobic polyolefin fiber, material and method for preparation thereof
US5403426A (en) 1991-05-28 1995-04-04 Hercules Incorporated Process of making cardable hydrophobic polypropylene fiber
EP0552013A2 (en) 1992-01-13 1993-07-21 Hercules Incorporated Thermally bondable fiber for high strength non-woven fabrics
US5629080A (en) 1992-01-13 1997-05-13 Hercules Incorporated Thermally bondable fiber for high strength non-woven fabrics
US5540953A (en) 1992-02-14 1996-07-30 Hercules Incorporated Process of preparing fabric comprising hydrophobic polyolefin fibers
US5296289A (en) 1992-04-29 1994-03-22 Collins Loren M Stretchable spun bonded nonwoven web and method
US5620776A (en) 1992-12-24 1997-04-15 James River Corporation Of Virginia Embossed tissue product with a plurality of emboss elements
US5656132A (en) 1993-06-24 1997-08-12 Kimberly-Clark Worldwide, Inc. Soft tissue
EP0630996A2 (en) 1993-06-24 1994-12-28 Hercules Incorporated Skin-core high thermal bond strength fiber on melt spin system
US5705119A (en) 1993-06-24 1998-01-06 Hercules Incorporated Process of making skin-core high thermal bond strength fiber
US5534208A (en) 1993-09-15 1996-07-09 Foamex L.P. Three dimensional surface shaping of synthetic foam pads by continuous rotary process
US5580423A (en) 1993-12-20 1996-12-03 The Procter & Gamble Company Wet pressed paper web and method of making the same
US5622734A (en) 1994-03-14 1997-04-22 Kimberly-Clark Corporation Apparatus for producing a crimp-bonded fibrous cellulosic laminate
EP0719879A2 (en) 1994-12-19 1996-07-03 Hercules Incorporated Process for producing fibers for high strength non-woven materials, and the resulting fibers and non-wovens
US5882562A (en) 1994-12-19 1999-03-16 Fiberco, Inc. Process for producing fibers for high strength non-woven materials
WO1997037065A1 (en) 1996-03-29 1997-10-09 Hercules Incorporated Polypropylene fibers and items made therefrom
US5985193A (en) 1996-03-29 1999-11-16 Fiberco., Inc. Process of making polypropylene fibers
WO1998015685A1 (en) 1996-10-09 1998-04-16 Hercules Incorporated Ester lubricants as hydrophobic fiber finishes

Non-Patent Citations (20)

* Cited by examiner, † Cited by third party
Title
"Cut strip test" in ASTM D-1682-64 (Re-Appproved 1975), pp. 255-260.
American National Standard, Standard Test Methods for Breaking Load and Elongation of Textile Fabrics<1>, ASTM D-1682-64 (Reapproved 1975), pp. 255-260.
American National Standard, Standard Test Methods for Breaking Load and Elongation of Textile Fabrics1, ASTM D-1682-64 (Reapproved 1975), pp. 255-260.
Hercules Bonding Pattern 004.
Hercules Engraving Pattern 010.
Hercules Engraving Pattern 011-With Logo.
Hercules Engraving Pattern 018.
Legare, R.J., 1986 TAPPI, Synthetic Fibers for Wet System and Thermal Bonding Applications, Boston Park Plaza Hotel & Towers, Boston, Mass., Oct. 9-10, 1986, " Thermal Bonding of Polypropylene Fibers in Nonwovens", pp. 1-13 and attached Tables and Figures.
Overbeck & Co., Design No. 1174.
Overbeck & Co., Design No. 1557.
Overbeck & Co., Design No. 2403.
Overbeck & Co., Design No. 2586.
Overbeck & Co., Design No. 3388.
Overbeck & Co., Design No. 3780.
Overbeck & Co., Design No. 3933.
Overbeck & Co., Design No. 4759.
Overbeck & Co., Design No. 6080.
Overbeck & Co., Design No. 776.
Overbeck & Co., Design No. 982.
Trent et al., in Macromolecules, vol. 16, No. 4; 1983; "Ruthenium Tetroxide Staining of Polymers for Electron Microscopy".

Cited By (25)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US20090123707A1 (en) * 2004-12-14 2009-05-14 Henry Skoog Embossed Nonwoven Fabric
US20060128247A1 (en) * 2004-12-14 2006-06-15 Kimberly-Clark Worldwide, Inc. Embossed nonwoven fabric
US8425729B2 (en) 2004-12-14 2013-04-23 Kimberly-Clark Worldwide, Inc. Embossed nonwoven fabric
US20070048498A1 (en) * 2005-08-29 2007-03-01 Cree James W Apertured Laminate and Method of Making
US7695799B2 (en) 2005-08-29 2010-04-13 Advantage Creation Enterprise Llc Apertured laminate and method of making
US20070249253A1 (en) * 2006-04-24 2007-10-25 Piero Angeli Elastic laminate comprising elastic substrate between extensible webs and method for making
US20100305543A1 (en) * 2007-08-16 2010-12-02 Frantisek Klaska Nonwoven fabric and method for the production thereof
US8664128B2 (en) 2008-01-30 2014-03-04 Advantage Creation Enterprise Llc Elastic laminate and method of making
US20090191779A1 (en) * 2008-01-30 2009-07-30 Cree James W Elastic laminate and method of making
US9067334B2 (en) 2009-03-24 2015-06-30 Advantage Creation Enterprise Llc Embossed textured webs and method for making
US10729597B2 (en) 2009-03-24 2020-08-04 Advantage Creation Enterprise Llc Embossed textured webs and method for making
US9849602B2 (en) 2009-12-18 2017-12-26 Advantage Creation Enterprise Llc Method for making extrusion coated perforated nonwoven web
US10821622B2 (en) 2009-12-18 2020-11-03 Advantage Creation Enterprise Llc Extrusion coated perforated nonwoven web and method for making
US20110151185A1 (en) * 2009-12-18 2011-06-23 Cree James W Extrusion coated perforated nonwoven web and method for making
US10028866B2 (en) 2011-03-25 2018-07-24 The Procter & Gamble Company Article with nonwoven web component formed with loft-enhancing calender bond shapes and patterns
US9408761B2 (en) 2011-03-25 2016-08-09 The Procter & Gamble Company Article with nonwoven web component formed with loft-enhancing calendar bond shapes and patterns
US9523164B2 (en) 2012-04-27 2016-12-20 Providencia Usa, Inc. Nonwoven fabric with bonding pattern
US9096961B2 (en) 2012-04-27 2015-08-04 Providencia Usa, Inc. Nonwoven wipe with bonding pattern
USD714560S1 (en) 2012-09-17 2014-10-07 The Procter & Gamble Company Sheet material for an absorbent article
USD702047S1 (en) 2012-10-15 2014-04-08 Polymer Group, Inc. Nonwoven fabric
US10828209B2 (en) 2015-12-16 2020-11-10 Avintiv Specialty Materials Inc. Soft nonwoven fabric and method of manufacturing thereof
US20180002851A1 (en) * 2016-03-10 2018-01-04 Reifenhaeuser Gmbh & Co. Kg Maschinenfabrik Weldable spunbond fabric, method of making same, and packaging made therefrom
US20210054550A1 (en) * 2016-03-10 2021-02-25 Claudio Cinquemani Method of making a spun-bonded nonwoven for packaging
USD907931S1 (en) * 2018-05-22 2021-01-19 Berry Global, Inc. Nonwoven fabric
USD907930S1 (en) * 2018-05-22 2021-01-19 Berry Global, Inc. Nonwoven fabric

Also Published As

Publication number Publication date
EP1144741A2 (en) 2001-10-17
WO2000004215A2 (en) 2000-01-27
AU4953399A (en) 2000-02-07
WO2000004215A3 (en) 2001-11-15
CA2336834A1 (en) 2000-01-27
CN1321119A (en) 2001-11-07
EP1144741A3 (en) 2002-03-06
JP2002522648A (en) 2002-07-23

Similar Documents

Publication Publication Date Title
US6752947B1 (en) Method and apparatus for thermal bonding high elongation nonwoven fabric
US20220145503A1 (en) Liquid Barrier Nonwoven Fabrics with Ribbon-Shaped Fibers
US20190062970A1 (en) Extensible nonwoven fabric
US6458726B1 (en) Polypropylene fibers and items made therefrom
EP2559793B1 (en) Composite crimp fiber, and non-woven fabric comprising the fiber
EP1264024B1 (en) Multicomponent apertured nonwoven
US6368990B1 (en) Fabrics formed of hollow filaments and fibers and methods of making the same
EP2298976B1 (en) Improved fibers for polyethylene nonwoven fabric
JP4599366B2 (en) A flexible and extensible nonwoven web containing fibers with high melt flow rate
EP2343406B1 (en) Crimped composite fiber, and non-woven fabric comprising the fiber
RU2731772C2 (en) Non-woven laminate fabric comprising a layer and spunbond layers aerodynamically sprayed from the melt
US20010005662A1 (en) Nonwoven fabrics and fabric laminates from multiconstituent polyolefin fibers
EP1354091B1 (en) Thermally bonded fabrics and method of making same
EP3419577B1 (en) Nonwoven fabrics with additive enhancing barrier properties
AU742081B2 (en) Nonwoven webs having improved softness and barrier properties
US10415157B2 (en) Eccentric hollow conjugated continuous fiber, continuous-fiber nonwoven fabric made therefrom and uses thereof
CA2489353C (en) Spinnerette and process for fiber production
CN113348277A (en) Spun-bonded nonwoven fabric, method for producing spun-bonded nonwoven fabric, and embossing roll
JP7138197B2 (en) Spunbond nonwoven fabric, sanitary material, and method for producing spunbond nonwoven fabric
JP2022135776A (en) Nonwoven fabric, nonwoven fabric laminate, and absorbent article

Legal Events

Date Code Title Description
AS Assignment

Owner name: FIBERVISIONS INCORPORATED, DELAWARE

Free format text: ASSIGNMENT OF ASSIGNORS INTEREST;ASSIGNORS:LANIGAN, WILLIAM ROBERT;LEGARE, RICHARD J.;SIBAL, SHIV;REEL/FRAME:009503/0865;SIGNING DATES FROM 19981002 TO 19981005

AS Assignment

Owner name: BANK OF AMERICA, N.A., AS COLLATERAL AGENT, NORTH

Free format text: NOTICE OF GRANT OF SECURITY INTEREST;ASSIGNORS:HERCULES INCORPORATED;HERCULES CREDIT, INC.;HERCULES FLAVOR, INC.;AND OTHERS;REEL/FRAME:011468/0319

Effective date: 20001114

AS Assignment

Owner name: CREDIT SUISSE FIRST BOSTON, AS COLLATERAL AGENT, N

Free format text: SECURITY INTEREST;ASSIGNOR:HERCULES INCORPORATED;REEL/FRAME:013625/0233

Effective date: 20021220

AS Assignment

Owner name: AQUALON COMPANY, DELAWARE

Free format text: RELEASE OF SECURITY INTEREST;ASSIGNOR:BANK OF AMERICA, N.A., AS COLLATERAL AGENT;REEL/FRAME:013680/0148

Effective date: 20021219

Owner name: ATHENS HOLDINGS, INC., DELAWARE

Free format text: RELEASE OF SECURITY INTEREST;ASSIGNOR:BANK OF AMERICA, N.A., AS COLLATERAL AGENT;REEL/FRAME:013680/0148

Effective date: 20021219

Owner name: BETZDEARBORN CHINA, LTD., DELAWARE

Free format text: RELEASE OF SECURITY INTEREST;ASSIGNOR:BANK OF AMERICA, N.A., AS COLLATERAL AGENT;REEL/FRAME:013680/0148

Effective date: 20021219

Owner name: BETZDEARBORN EUROPE, INC., DELAWARE

Free format text: RELEASE OF SECURITY INTEREST;ASSIGNOR:BANK OF AMERICA, N.A., AS COLLATERAL AGENT;REEL/FRAME:013680/0148

Effective date: 20021219

Owner name: BETZDEARBORN INTERNATIONAL, INC., DELAWARE

Free format text: RELEASE OF SECURITY INTEREST;ASSIGNOR:BANK OF AMERICA, N.A., AS COLLATERAL AGENT;REEL/FRAME:013680/0148

Effective date: 20021219

Owner name: BETZDEARBORN, INC., DELAWARE

Free format text: RELEASE OF SECURITY INTEREST;ASSIGNOR:BANK OF AMERICA, N.A., AS COLLATERAL AGENT;REEL/FRAME:013680/0148

Effective date: 20021219

Owner name: BL CHEMICALS INC., DELAWARE

Free format text: RELEASE OF SECURITY INTEREST;ASSIGNOR:BANK OF AMERICA, N.A., AS COLLATERAL AGENT;REEL/FRAME:013680/0148

Effective date: 20021219

Owner name: BL TECHNOLOGIES, INC., DELAWARE

Free format text: RELEASE OF SECURITY INTEREST;ASSIGNOR:BANK OF AMERICA, N.A., AS COLLATERAL AGENT;REEL/FRAME:013680/0148

Effective date: 20021219

Owner name: BLI HOLDING CORPORATION, DELAWARE

Free format text: RELEASE OF SECURITY INTEREST;ASSIGNOR:BANK OF AMERICA, N.A., AS COLLATERAL AGENT;REEL/FRAME:013680/0148

Effective date: 20021219

Owner name: CHEMICAL TECHNOLOGIES INDIA, LTD., DELAWARE

Free format text: RELEASE OF SECURITY INTEREST;ASSIGNOR:BANK OF AMERICA, N.A., AS COLLATERAL AGENT;REEL/FRAME:013680/0148

Effective date: 20021219

Owner name: COVINGTON HOLDINGS, INC., DELAWARE

Free format text: RELEASE OF SECURITY INTEREST;ASSIGNOR:BANK OF AMERICA, N.A., AS COLLATERAL AGENT;REEL/FRAME:013680/0148

Effective date: 20021219

Owner name: D R C LTD., DELAWARE

Free format text: RELEASE OF SECURITY INTEREST;ASSIGNOR:BANK OF AMERICA, N.A., AS COLLATERAL AGENT;REEL/FRAME:013680/0148

Effective date: 20021219

Owner name: EAST BAY REALTY SERVICES, INC., DELAWARE

Free format text: RELEASE OF SECURITY INTEREST;ASSIGNOR:BANK OF AMERICA, N.A., AS COLLATERAL AGENT;REEL/FRAME:013680/0148

Effective date: 20021219

Owner name: FIBERVISIONS INCORPORATED, DELAWARE

Free format text: RELEASE OF SECURITY INTEREST;ASSIGNOR:BANK OF AMERICA, N.A., AS COLLATERAL AGENT;REEL/FRAME:013680/0148

Effective date: 20021219

Owner name: FIBERVISIONS PRODUCTS, INC., DELAWARE

Free format text: RELEASE OF SECURITY INTEREST;ASSIGNOR:BANK OF AMERICA, N.A., AS COLLATERAL AGENT;REEL/FRAME:013680/0148

Effective date: 20021219

Owner name: FIBERVISIONS, L.L.C., DELAWARE

Free format text: RELEASE OF SECURITY INTEREST;ASSIGNOR:BANK OF AMERICA, N.A., AS COLLATERAL AGENT;REEL/FRAME:013680/0148

Effective date: 20021219

Owner name: FIBERVISIONS, L.P., DELAWARE

Free format text: RELEASE OF SECURITY INTEREST;ASSIGNOR:BANK OF AMERICA, N.A., AS COLLATERAL AGENT;REEL/FRAME:013680/0148

Effective date: 20021219

Owner name: HERCULES CHEMICAL CORPORATION, DELAWARE

Free format text: RELEASE OF SECURITY INTEREST;ASSIGNOR:BANK OF AMERICA, N.A., AS COLLATERAL AGENT;REEL/FRAME:013680/0148

Effective date: 20021219

Owner name: HERCULES COUNTRY CLUB, INC., DELAWARE

Free format text: RELEASE OF SECURITY INTEREST;ASSIGNOR:BANK OF AMERICA, N.A., AS COLLATERAL AGENT;REEL/FRAME:013680/0148

Effective date: 20021219

Owner name: HERCULES CREDIT, INC., DELAWARE

Free format text: RELEASE OF SECURITY INTEREST;ASSIGNOR:BANK OF AMERICA, N.A., AS COLLATERAL AGENT;REEL/FRAME:013680/0148

Effective date: 20021219

Owner name: HERCULES EURO HOLDINGS, LLC, DELAWARE

Free format text: RELEASE OF SECURITY INTEREST;ASSIGNOR:BANK OF AMERICA, N.A., AS COLLATERAL AGENT;REEL/FRAME:013680/0148

Effective date: 20021219

Owner name: HERCULES FINANCE COMPANY, DELAWARE

Free format text: RELEASE OF SECURITY INTEREST;ASSIGNOR:BANK OF AMERICA, N.A., AS COLLATERAL AGENT;REEL/FRAME:013680/0148

Effective date: 20021219

Owner name: HERCULES FLAVOR, INC., DELAWARE

Free format text: RELEASE OF SECURITY INTEREST;ASSIGNOR:BANK OF AMERICA, N.A., AS COLLATERAL AGENT;REEL/FRAME:013680/0148

Effective date: 20021219

Owner name: HERCULES INCORPORATED, DELAWARE

Free format text: RELEASE OF SECURITY INTEREST;ASSIGNOR:BANK OF AMERICA, N.A., AS COLLATERAL AGENT;REEL/FRAME:013680/0148

Effective date: 20021219

Owner name: HERCULES INTERNATIONAL LIMITED, DELAWARE

Free format text: RELEASE OF SECURITY INTEREST;ASSIGNOR:BANK OF AMERICA, N.A., AS COLLATERAL AGENT;REEL/FRAME:013680/0148

Effective date: 20021219

Owner name: HERCULES INTERNATIONAL LIMITED, L.L.C., DELAWARE

Free format text: RELEASE OF SECURITY INTEREST;ASSIGNOR:BANK OF AMERICA, N.A., AS COLLATERAL AGENT;REEL/FRAME:013680/0148

Effective date: 20021219

Owner name: HERCULES INVESTMENTS, LLC, DELAWARE

Free format text: RELEASE OF SECURITY INTEREST;ASSIGNOR:BANK OF AMERICA, N.A., AS COLLATERAL AGENT;REEL/FRAME:013680/0148

Effective date: 20021219

Owner name: HERCULES SHARED SERVICES CORPORATION, DELAWARE

Free format text: RELEASE OF SECURITY INTEREST;ASSIGNOR:BANK OF AMERICA, N.A., AS COLLATERAL AGENT;REEL/FRAME:013680/0148

Effective date: 20021219

Owner name: HISPAN CORPORATION, DELAWARE

Free format text: RELEASE OF SECURITY INTEREST;ASSIGNOR:BANK OF AMERICA, N.A., AS COLLATERAL AGENT;REEL/FRAME:013680/0148

Effective date: 20021219

Owner name: WSP, INC., DELAWARE

Free format text: RELEASE OF SECURITY INTEREST;ASSIGNOR:BANK OF AMERICA, N.A., AS COLLATERAL AGENT;REEL/FRAME:013680/0148

Effective date: 20021219

STCF Information on status: patent grant

Free format text: PATENTED CASE

AS Assignment

Owner name: CREDIT SUISSE, NEW YORK

Free format text: SECOND LIEN SECURITY AGREEMENT;ASSIGNOR:FIBERVISIONS, L.P.;REEL/FRAME:017537/0220

Effective date: 20060426

Owner name: CREDIT SUISSE, NEW YORK

Free format text: FIRST LIEN SECURITY AGREEMENT;ASSIGNOR:FIBERVISIONS, L.P.;REEL/FRAME:017537/0201

Effective date: 20060426

AS Assignment

Owner name: HERCULES INCORPORATED, DELAWARE

Free format text: RELEASE BY SECURED PARTY;ASSIGNOR:CREDIT SUISSE;REEL/FRAME:018087/0723

Effective date: 20060331

FPAY Fee payment

Year of fee payment: 4

AS Assignment

Owner name: HERCULES INCORPORATED, DELAWARE

Free format text: PATENT TERMINATION CS-013625-0233;ASSIGNOR:CREDIT SUISSE, CAYMAN ISLANDS BRANCH;REEL/FRAME:021901/0585

Effective date: 20081113

AS Assignment

Owner name: BANK OF AMERICA, N.A., AS ADMINISTRATIVE AGENT, IL

Free format text: NOTICE OF GRANT OF SECURITY INTEREST IN PATENTS;ASSIGNOR:FIBERVISIONS L.P.;REEL/FRAME:025848/0826

Effective date: 20110224

AS Assignment

Owner name: FIBERVISIONS, L.P., GEORGIA

Free format text: RELEASE OF FIRST LIEN SECURITY INTEREST IN INTELLECTUAL PROPERTY COLLATERAL AT REEL/FRAME NO. 17537/0201;ASSIGNOR:CREDIT SUISSE AG, CAYMAN ISLANDS BRANCH (F/K/A CREDIT SUISSE, CAYMAN ISLANDS BRANCH);REEL/FRAME:025877/0477

Effective date: 20110224

Owner name: FIBERVISIONS, L.P., GEORGIA

Free format text: RELEASE OF SECOND LIEN SECURITY INTEREST IN INTELLECTUAL PROPERTY COLLATERAL AT REEL/FRAME NO. 17537/0220;ASSIGNOR:CREDIT SUISSE AG, CAYMAN ISLANDS BRANCH (F/K/A CREDIT SUISSE, CAYMAN ISLANDS BRANCH);REEL/FRAME:025877/0491

Effective date: 20110224

AS Assignment

Owner name: FIBERVISIONS MANUFACTURING COMPANY, GEORGIA

Free format text: CHANGE OF NAME;ASSIGNOR:FIBERVISIONS INCORPORATED;REEL/FRAME:026305/0334

Effective date: 20090617

AS Assignment

Owner name: FIBERVISIONS, L.P., GEORGIA

Free format text: ASSIGNMENT OF ASSIGNORS INTEREST;ASSIGNOR:FIBERVISIONS MANUFACTURING COMPANY;REEL/FRAME:026587/0265

Effective date: 20110701

FPAY Fee payment

Year of fee payment: 8

AS Assignment

Owner name: FIBERVISIONS, L.P., GEORGIA

Free format text: TERMINATION AND RELEASE OF SECURITY INTEREST IN PATENTS;ASSIGNOR:BANK OF AMERICA, N.A., AS ADMINISTRATIVE AGENT;REEL/FRAME:027489/0770

Effective date: 20120106

FPAY Fee payment

Year of fee payment: 12